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  • 1
    ISSN: 1420-9071
    Schlagwort(e): Insulin ; insulin-like growth factor ; Bombyx mori ; ovary ; neurosecretory peptide ; Oligotex reverse transcription-polymerase chain reaction
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract Bombyxin is a 5 kDa insulin-related peptide produced in four pairs of medial neurosecretory cells in the brain of the silkmothBombyx mori. We demonstrate here the presence of bombyxin mRNA in tissues other than brain: ganglia, epidermis, testis, ovary, fat body, silk gland, Malpighian tubule, midgut, and hindgut of theBombyx fifth instar larvae. Bombyxin mRNA was detected by Oligotex reverse transcription-polymerase chain reaction (RT-PCR), a rapid and simple procedure of reverse transcription-PCR, and in situ hybridization. The Oligotex RT-PCR method effectively eliminated the contaminating DNA in RNA samples and amplified bombyxin mRNA efficiently. In situ hybridization of theBombyx ovary clearly demonstrated the localization of the bombyxin mRNA in the ovariole. The present study is the first demonstration of expression of brain neurosecretory peptide in tissues other than the central nervous system in insects at RNA level.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Virchows Archiv 428 (1996), S. 177-185 
    ISSN: 1432-2307
    Schlagwort(e): Diabetic Chinese hamster ; Pancreatic beta cell ; Immunocytochemistry ; Insulin ; GLUT2 glucose transporter
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The diabetic Chinese hamster is a well-established animal model for NIDDM with a defective glucose-induced insulin secretory response. In the pancreas of nondiabetic hamsters, the GLUT2 glucose transporter was localized in the plasma membrane of insulin-positive beta cells. At variance with the rat, immunoreactivity was also detected in the cytoplasm. Other islet cell types were not GLUT2 positive. GLUT2 immunoreactivity was already significantly reduced in beta cells from mildly diabetic animals in spite of a normal insulin immunoreactivity. In severely diabetic animals the majority of the beta cells had lost GLUT2 immunostaining. This observation was confirmed in a Western blot analysis of the GLUT2 protein in isolated pancreatic islets. Only beta cells that were densely immunostained for insulin were still GLUT2 positive. However, around 40% of the beta cells devoid of GLUT2 immunoreactivity were still insulin immunoreactive. Thus, the loss of GLUT2 immunoreactivity, which is an important component of the glucose recognition apparatus of the pancreatic beta cell, is an early indicator of beta cell dysfunction before the development of degenerative lesions or the loss of insulin immunoreactivity. GLUT2 loss may be important in the deterioration of glucose-induced insulin secretion in the diabetic Chinese hamster.
    Materialart: Digitale Medien
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  • 3
    ISSN: 1432-0568
    Schlagwort(e): Key words Gastro-entero-endocrine cells ; Enteric nerve fibers ; Insulin ; Glucagon ; Somatostatin ; Pancreatic polypeptide ; Neuropeptide Y ; Insulin-like growth factor I ; Pancreastatin ; Neurotensin ; Substance P ; Gastrin ; Cholecystokinin ; Vasoactive intetinal polypeptide ; Serotonin ; Development ; Scophthalmus maximus
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract  The ontogeny of endocrine cells and nerve fibers containing immunoreactivities for 12 regulatory peptides and serotonin was studied in the digestive tract of a flatfish, the turbot (Scophthalmus maximus), using antisera specific for mammalian and teleostean hormones. Transient insulin-immunoreactive (-IR) endocrine cells were detected from day 5 to day 10 in stomach and intestine I. Somatostatin (SOM)-IR cells appeared at day 8 in the stomach anlage and intestine I. In contrast to the islet cells, they reacted with antisera against mammalian (m) SOM-14 and salmon (s) SOM-25. Infrequent nerve fibers reacting only with anti-mSOM-14 appeared around day 24. Thus, different forms of SOM seem to be present in the gastro-entero-pancreatic system and the enteric nervous system. Neuropeptide Y (NPY)-, salmon pancreatic polypeptide (sPP)- and mPP-immunoreactivities coexisted thoughout development. In entero-endocrine cells, NPY/PP-immunoreactivity was first observed at day 8 and around day 24 in enteric nerve fibers. Glucagon (GLUC)-IR entero-endocrine cells appeared at day 5. No coexistence of NPY/PP- and GLUC-immunoreactivities was observed. The first insulin-like growth factor I (IGF-I)-IR cells were identified around day 8. They seemed to contain none of the other peptides. Their number and distribution exhibited great interindividual differences. Vasoactive intestinal polypeptide (VIP)-IR entero-endocrine cells appeared as late as around day 24. The first VIP-IR nerve fibers, however, were identified at day 5. Infrequent neurotensin (NT)-IR cells appeared along the intestine around day 10 and NT-IR nerve fibers at day 17. The first serotonin (SER)-IR cells were observed in the stomach anlage around day 10 and SER-IR nerve fibers at day 15 thoughout the gastro-intestinal tract. Gastrin (GAS)/cholecystokinin (CCK)-IR cells appeared around day 11 in stomach and intestine I. The first substance P (SP)-IR enteric nerve fibers were detected around day 8 and SP-IR endocrine cells at day 11. Pancreastatin (PST)-IR cells were identified in the stomach anlage and intestine I around day 8 and contained NT-, GAS/CCK- and SER-immunoreactivities in coexistence. Thus, several developmental phases can be distinguished: (1) at the onset of exogenous feeding only transient INS-IR cells and VIP-IR nerve fibers are present; (2) a differentiated entero-endocrine system establishes during the early phase of exogenous feeding; (3) before the final differentiation of stomach and gut GAS/CCK-IR cells appear; (4) after metamorphosis most of the different types of regulatory peptide-containing nerve fibers develop, probably setting up the fine regulation of gastro-intestinal blood flow and motility.
    Materialart: Digitale Medien
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  • 4
    ISSN: 1432-0428
    Schlagwort(e): Insulin ; small GTPases ; GLUT4 ; translocation ; adipocytes
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The small guanosine 5′-triphosphate (GTP)ase Rab4 has been suggested to play a role in insulin-induced GLUT4 translocation. Under insulin stimulation, GLUT4 translocates to the plasma membranes, while Rab4 leaves the GLUT4-containing vesicles and becomes cytosolic. Rab proteins cycle between a GTP-bound active form and a guanosine 5′-diphosphate (GDP)-bound inactive form. The intrinsic GTPase activity of Rab proteins is low and the interconversion between the two forms is dependent on accessory factors. In the present work, we searched for a GTPase activating protein (GAP) for Rab4 in 3T3-L1 adipocytes. We used a glutathione-S-transferase (GST)-Rab4 protein which possesses the properties of a small GTPase (ability to bind GDP and GTP and to hydrolyse GTP) and can be isolated in a rapid and efficient way. This GAP activity was observed in 3T3-L1 adipocyte lysates, and was able to accelerate the hydrolysis of the [α-32P]GTP bound to GST-Rab4 into [α-32P]GDP. This activity, tentatively called Rab4-GAP, was also present in 3T3-L1 fibroblasts. The Rab4-GAP activity was present in total membrane fractions and nearly undetectable in cytosol. Following subcellular fractionation, Rab4-GAP was found to be enriched in plasma membranes when compared to internal microsomes. Insulin treatment of the cells had no effect on the total Rab4-GAP activity or on its subcellular localization. Taking our results together with the accepted model of Rab cycling in intracellular traffic, we propose that Rab4-GAP activity plays a role in the cycling between the GTP- and GDP-bound forms of Rab4, and thus possibly in the traffic of GLUT4-containing vesicles.
    Materialart: Digitale Medien
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  • 5
    ISSN: 1432-0428
    Schlagwort(e): Insulin ; insulin receptor substrate-1 ; phosphoinositide 3-kinase ; signal transduction ; phosphotyrosine ; enzyme activation ; conformational change ; Fao cells
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Phosphoinositide 3-kinase (PI3-kinase) plays a crucial role in insulin signal transduction. We studied the molecular mechanism of the insulin-induced activation of PI3-kinase in rat hepatoma Fao cells using an antibody against the 110-kDa catalytic subunit (p110) and two against the 85-kDa regulatory subunit (p85α). PI3-kinase activity increased 1.6-fold in anti-p85 immunoprecipitates after insulin stimulation, whereas it did not increase when cell lysates were first immunoprecipitated with anti-phosphotyrosine or anti-insulin receptor substrate-1 (IRS-1), then with anti-p85, suggesting that the PI3-kinase which associates with tyrosyl phosphoproteins including IRS-1 is responsible for the increase in kinase activity. The activated PI3-kinase molecules constituted 4–6% of the total PI3-kinase, and their specific activity was 11–14 times higher than that of the basal state. Anti-p110 recognized the catalytically active form of p110, and immunoprecipitated p110 only after exposure to insulin. Hence, the epitope of anti-p110, P200-C215, seems to be included in the portion of p110, the conformation of which is changed by insulin stimulation. We conclude that, in response to insulin stimulation, only a small fraction of p85 in the PI3-kinase pool associates with tyrosyl phosphoproteins including IRS-1, and that the specific activity of p110 is increased presumably through a conformational change including the P200-C215 region.
    Materialart: Digitale Medien
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  • 6
    ISSN: 1423-0127
    Schlagwort(e): Endothelin-1 ; Insulin ; Protein Kinase FA/GSK-3α ; MAP kinase signaling pathway ; Rat adipocytes
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract In this study, we investigate the effects of endothelin-1 (ET-1) and insulin on the cellular activity of protein kinase FA/glycogen synthase kinase-3α (kinase FA/GSK-3α) in rat adipocytes. The cellular activity of kinase FA/GSK-3α is inhibited to ∼ 50% of control within 30 min when cells are treated with 1 nM ET-1 at 37°C; in addition, significant inhibition to ∼ 60% of control is observed at as low as 1 pM ET-1. Conversely, ET-1 at concentrations up to 1 nM has no direct effect on purified kinase FA/GSK-3α in vitro. Immunoblotting analysis further reveals that the protein level of this kinase is not significantly changed when treated with 1 nM ET-1 for 30 min. Similar to ET-1, insulin as low as 10 nM can also induce inactivation of kinase FA/GSK-3α to ∼ 50% of control in adipocytes when processed under identical conditions. Most importantly, when treated with both insulin and ET-1, the activity of kinase FA/GSK-3α can be decreased only to ∼ 50% of control. Taken together, the results provide initial evidence that ET-1 and insulin may regulate this important multisubstrate/multifunctional protein kinase in a common signaling pathway in cells.
    Materialart: Digitale Medien
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  • 7
    ISSN: 1432-0428
    Schlagwort(e): Insulin ; mediator ; d-chiro-inositol ; euglycaemia ; manganese
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary We compared the effects of infusing a chemically defined chiro-inositol glycan putative insulin mediator with an equivalent dose of insulin in low-dose (45 mg/kg) streptozotocin diabetic rats. Insulin decreased plasma glucose levels from 17.32±0.17 to 3.96±0.064 mmol/l (p〈0.0002) in 120 min, a decrease of 77.13%, while the putative mediator promoted a decrease in plasma glucose from 14.85±0.084 to 7.22±0.13 mmol/l (p〈0.007) in 60 min. The putative mediator maintained euglycaemia over the ensuing 60 min with a plasma glucose level of 7.01±0.10 mmol/l at 120 min. Thus, insulin further reduced the plasma glucose from euglycaemia at 60 min to produce hypoglycaemia at 120 min. The lack of production of hypoglycaemia by the putative mediator can be explained by its inhibition of glucose-stimulated insulin secretion by the islet beta cells, thus providing a potential negative feedback regulatory mechanism; or by its selective action on muscle to increase glycogen synthesis. The significance of these results in terms of future directions in drug design is herein considered.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Springer
    Cellular and molecular life sciences 52 (1996), S. 421-425 
    ISSN: 1420-9071
    Schlagwort(e): Insulin ; fatty acids ; insulin-like growth factors ; Cori cycle
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract Insulin can influence rates of glucose utilization by muscle and possibly other tissues via both direct and indirect effects. It can control the rate of fatty acid mobilization from adipose tissue and the rate of fatty acid oxidation in muscle, and the latter inhibits glucose utilization and oxidation. Insulin may influence the levels of insulin-like growth factors I and II, both of which have effects on rates of glucose utilization by muscle. The intertissue cycle between glucose and lactate — the Cori cycle, which is influenced by insulin — may provide another novel mechanism for control of blood glucose. How far other anti-insulin hormones affect these processes is not clear.
    Materialart: Digitale Medien
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  • 9
    ISSN: 1432-041X
    Schlagwort(e): Key words Hydra ; Insulin ; Development ; Receptor ; Evolution
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract  A gene encoding a receptor protein-tyrosine kinase closely related to the vertebrate insulin receptor has been identified in the Cnidarian Hydra vulgaris. The gene is expressed in both epithelial layers of the adult polyp. A particularly high level of expression is seen in the ectoderm of the proximal portions of the tentacles and in a ring of ectodermal cells at the border between the foot basal disk and body column. The expression pattern of the gene in asexual buds is dynamic; expression is high throughout the newly emerging bud but the area of high expression becomes restricted to the apex as the bud lengthens. When the bud begins hypostome and tentacle formation, a high level of expression appears at the bases of the emerging tentacles. Finally, a ring of high expression appears just above the foot of the bud, completing the pattern seen in the adult polyp. The presence of this receptor and its pattern of expression suggested that an endogenous molecule related to insulin plays a role in regulating cell division in the body column and in differentiation of the tentacle and foot cells in Hydra, with the switch between the two being determined by the level of the receptor. Treatment of Hydra polyps with mammalian insulin caused an increase in the number of ectodermal and endodermal cells undergoing DNA synthesis.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Springer
    Cellular and molecular life sciences 52 (1996), S. 769-773 
    ISSN: 1420-9071
    Schlagwort(e): Insulin ; imprinting ; Tetrahymena ; phagocytosis ; insulin receptor
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract Receptor-mediated endocytosis byTetrahvmena pyriformis was studied using tetramethylrhodamine isothiocyanate-labeled concanavalin A (TRITC-Con A) with fluorescence and confocal microscopy. In the presence of insulin, or 24 h after insulin pretreatment (hormonal imprinting), the binding and uptake of TRITC-Con A increased when compared to controls, owing to the binding of TRITC-Con A to sugar oligomers of insulin recptors. Mannose inhibited the binding of Con A, thus demonstrating the specificity of binding. Histamine, a phagocytosis-promoting factor in mammals andTetrahymena, and galactose, did not influence the uptake of TRITC-Con A.
    Materialart: Digitale Medien
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  • 11
    Digitale Medien
    Digitale Medien
    Springer
    Cellular and molecular life sciences 52 (1996), S. 426-432 
    ISSN: 1420-9071
    Schlagwort(e): Insulin ; proinsulin ; insulin resistance ; metabolic syndrome ; triglycerides ; free fatty acids ; fat intake ; galanin
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract For better comprehension of the metabolic syndrome, it is necessary to differentiate the effect of insulin on glucose metabolism on the one hand, and on other metabolic activities on the other hand. Whereas glucose utilization is affected by insulin resistance, the effect of insulin on lipid metabolism, ion and aminoacid transport does not seem to be diminished. Lipid metabolism, however, seems to play a crucial role in the induction of the vicious cycle. Increased energy and fat ingestion may be due to an increased number of galanin secreting cells in the hypothalamus. The excessive fat intake results in an increased rate of release of insulin and increased influx of triglycerides into the blood. From these triglycerides an excess of free fatty acids is released by the action of lipoprotein lipase. The increased plasma free fatty acid level then results in insulin resistance affecting glucose metabolism. Also, these free fatty acids may impair the secretion of insulin. Induction of insulin resistance results in higher glucose levels, which may cause hyperinsulinemia. Hyperinsulinemia maintains the elevation of triglycerides. When diabetes becomes overt and elevated glucose levels prevail, the hyperinsulinism acts on the metabolic pathways which are still sensitive to insulin, namely lipid metabolism, aminoacid transport and ion transport.
    Materialart: Digitale Medien
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  • 12
    Digitale Medien
    Digitale Medien
    Springer
    Calcified tissue international 59 (1996), S. 492-495 
    ISSN: 1432-0827
    Schlagwort(e): Insulin ; Osteoblasts ; In vivo ; Calvariae ; Histomorphometry
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin , Physik
    Notizen: Abstract Recent clinical studies have established that bone density is related to both fat mass and circulating insulin levels. A direct action of insulin on the osteoblast may contribute to these relationships. Osteoblast-like cells have insulin receptors, and insulin has been shown to stimulate proliferation of these cells in vitro. However, it has not been possible to study the effects of insulin administration on bone in vivo because of the metabolic effects of insulin, particularly hypoglycemia. A model involving the local injection of insulin over one hemicalvaria of an adult mouse overcomes these difficulties and permits the histomorphometric study of insulin's action on bone. Insulin or vehicle was injected daily for 5 days over the right hemicalvariae of adult mice, and the animals were sacrificed 1 week later. All indices of bone formation were significantly increased in imsulin-treated hemicalvariae compared with the noninjected hemicalvariae. There was a 2.73±0.50-fold increase in osteoid area (P=0.0005), a 2.20±0.37-fold increase in osteoblast surface (P=0.021) and a 2.04±0.29-fold increase in osteoblast number (P=0.021). Indices of bone resorption tended to decline and mineralized bone area tended to increase in insulin-treated animals. The direct action of insulin on bone may contribute to the increased bone density seen in obesity and to the osteopenia of type I diabets, conditions associated with insulin excess and deficiency, respectively.
    Materialart: Digitale Medien
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  • 13
    ISSN: 1432-2013
    Schlagwort(e): Propionyl-l-carnitine ; Insulin ; Streptozotocin-induced diabetic rat ; Motor nerve ; conduction velocity ; Sciatic nerve blood flow ; Electroretinogram ; Sorbitol ; myo-Inositol
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The effect of an analogue ofl-carnitine, propionyl-l-carnitine, on the electroretinogram, motor nerve conduction velocity and nerve blood flow was determined in rats with streptozotocin-induced diabetes, and was compared with the effects of insulin alone or combined therapy. Oral administration of propionyl-l-carnitine (3 g/kg daily for 4 weeks) significantly increased caudal nerve motor conduction velocity and sciatic nerve blood flow in diabetic rats. There were no differences in the effects of insulin (8–10 U daily for 4 weeks), propionyl-l-carnitine and combined therapy. Although propionyl-l-carnitine significantly shortened the peak latency of the electroretinogram b-wave in diabetic rats, its effect was far weaker than that of insulin or combined therapy, with combined therapy producing the greatest improvement. These effects of propionyl-l-carnitine were accompanied by a decrease of serum lipid levels, an increase of the sciatic nerve carnitine content, and no changes of the tissue (nerve and retinal) sorbitol andmyo-inositol concentrations. In contrast, insulin significantly reduced the tissue sorbitol content and markedly increasedmyo-inositol. These findings suggest that propionyl-l-carnitine may improve diabetic neuropathy and retinopathy without influencing the polyol pathway, and that this beneficial effect may be mediated through the amelioration of microcirculation and tissue carnitine content, thus probably increasing fatty acid oxidation.
    Materialart: Digitale Medien
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  • 14
    Digitale Medien
    Digitale Medien
    Springer
    European journal of pediatrics 156 (1996), S. 1-2 
    ISSN: 1432-1076
    Schlagwort(e): Key words Neonatal diabetes mellitus ; Intra-uterine dystrophy ; Insulin ; Insulin-like growth factor␣I ; Fetal growth
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Materialart: Digitale Medien
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  • 15
    Digitale Medien
    Digitale Medien
    Springer
    European biophysics journal 24 (1996), S. 354-357 
    ISSN: 1432-1017
    Schlagwort(e): Cyclodextrin ; Insulin ; Dimer Dissociation ; Microcalorimetry ; Thermodynamics
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Physik
    Notizen: Abstract The energetics of dissociation of bovine insulin in aqueous solution have been investigated by sensitive dilution microcalorimetry. Cyclodextrins increase dissociation of insulin oligomers in a manner consistent with their interaction with protein side chains. For example, assuming monomer-dimer equilibrium, in the absence of cyclo-dextrins the calorimetric dilution data (25 °C, pH 2.5) indicate a dimer dissociation constant (Kdiss) of about 12 µM and an endothermic dissociation enthalpy (ΔHdiss) of +41 kJ mol−1. Addition of methyl-β-cyclodextrin (up to 200 mm) makes dissociation significantly more endothermic (ΔHdiss = 79 kJ mol−1) and reduces the apparent dimer dissociation constant by more than two orders of magnitude (Kdiss ≈ 1.7 mm). Qualitatively similar results are observed with α-cyclodextrin and other β-cyclodextrin derivatives. Cyclodextrin-induced insulin dissociation is also observed at pH 7.4.
    Materialart: Digitale Medien
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  • 16
    Digitale Medien
    Digitale Medien
    Springer
    Pflügers Archiv 431 (1996), S. 748-756 
    ISSN: 1432-2013
    Schlagwort(e): Benzamil ; Insulin ; Nonselective cation channel ; Na+ channel ; Alveolar cells ; Type II ; Single-channel recording
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The Na+ transport function of alveolar epithelium represents an important mechanism for clearance of fluid in air space at birth. I observed the activity of two types of amiloride-blockable Na+-permeant cation channels in the apical membrane of fetal distal lung epithelium cultured on permeable filters for 2 days after harvesting of the cells from Wistar rats of 20 days' gestation (term = 22 days). One type was a nonselective cation (NSC) channel and had a linear current/voltage (I/V) relationship with a single-channel conductance of 26.9 ± 0.8 pS (n = 5). The other type was highly Na+ selective (i.e. Na+ channel) and had an inwardly rectifyingI/V relationship with a single-channel conductance of 11.8 ± 0.2 pS (n = 5) around resting membrane potential. The NSC channel was more frequently observed (1.37 ± 0.15 per patch membrane;n = 73) than the Na+ channel (0.15 ± 0.40 per patch membrane;n = 73). However, the open probability of the NSC channel was smaller than that of the Na+ channel. Both types of the channels were activated by cytosolic Ca2+, however the sensitivity to cytosolic Ca2+ was much higher in the Na+ channel than in the NSC channel. Furthermore, both types of the channels were blocked by amiloride or benzamil. The half-maximal inhibitory concentration (IC50) of amiloride or benzamil of the Na+ channel was 1–2 μM, while that of NSC channel was less than 1 μM. Both channels were activated by insulin.
    Materialart: Digitale Medien
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  • 17
    ISSN: 1432-2013
    Schlagwort(e): Key words Propionyl-L-carnitine ; Insulin ; Streptozotocin-induced diabetic rat ; Motor nerve conduction velocity ; Sciatic nerve blood flow ; Electroretinogram ; Sorbitol ; myo-Inositol
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The effect of an analogue of L-carnitine, propionyl-L-carnitine, on the electroretinogram, motor nerve conduction velocity and nerve blood flow was determined in rats with streptozotocin-induced diabetes, and was compared with the effects of insulin alone or combined therapy. Oral administration of propionyl-L-carnitine (3 g/kg daily for 4 weeks) significantly increased caudal nerve motor conduction velocity and sciatic nerve blood flow in diabetic rats. There were no differences in the effects of insulin (8–10 U daily for 4 weeks), propionyl-L-carnitine and combined therapy. Although propionyl-L-carnitine significantly shortened the peak latency of the electroretinogram b-wave in diabetic rats, its effect was far weaker than that of insulin or combined therapy, with combined therapy producing the greatest improvement. These effects of propionyl-L-carnitine were accompanied by a decrease of serum lipid levels, an increase of the sciatic nerve carnitine content, and no changes of the tissue (nerve and retinal) sorbitol and myo-inositol concentrations. In contrast, insulin significantly reduced the tissue sorbitol content and markedly increased myo-inositol. These findings suggest that propionyl-L-carnitine may improve diabetic neuropathy and retinopathy without influencing the polyol pathway, and that this beneficial effect may be mediated through the amelioration of microcirculation and tissue carnitine content, thus probably increasing fatty acid oxidation.
    Materialart: Digitale Medien
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  • 18
    Digitale Medien
    Digitale Medien
    Springer
    Pflügers Archiv 432 (1996), S. 685-691 
    ISSN: 1432-2013
    Schlagwort(e): Key words Aldosterone ; Insulin ; IGF1 ; ADH ; Vasopressin
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The Madin-Darby canine kidney (MDCK) cell line forms an epithelial monolayer which expresses many of the morphological and functional properties of the renal collecting duct. The C7 subclone of the parent line forms an epithelium which expresses many of the characteristics of principal cells. The MDCK-C7 subclone forms a high-resistance epithelium that is capable of vectorial ion transport. We have found that this epithelium responds to aldosterone, antidiuretic hormone (ADH) and insulin like growth factor 1 (IGF1) with increases in amiloride-sensitive Na+ transport. The responses to aldosterone and ADH follow time-courses that are consistent with the action of these hormones in vivo. This is the first demonstration of IGF1-induced Na+ reabsorption in a mammalian model system. Interestingly, a maximal response to any one of these natriferic factors does not inhibit a subsequent response to another hormone. These studies indicate that the C7 subclone retains many of the natriferic responses of the native principal cells and is an ideal model for studying hormonal modulation of Na+ transport.
    Materialart: Digitale Medien
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  • 19
    Digitale Medien
    Digitale Medien
    Springer
    Pflügers Archiv 431 (1996), S. 748-756 
    ISSN: 1432-2013
    Schlagwort(e): Key words Benzamil ; Insulin ; Nonselective cation channel ; Na+ channel ; Alveolar cells ; Type II ; Single-channel recording
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The Na+ transport function of alveolar epithelium represents an important mechanism for clearance of fluid in air space at birth. I observed the activity of two types of amiloride-blockable Na+-permeant cation channels in the apical membrane of fetal distal lung epithelium cultured on permeable filters for 2 days after harvesting of the cells from Wistar rats of 20 days’ gestation (term = 22 days). One type was a nonselective cation (NSC) channel and had a linear current/voltage (I/V) relationship with a single-channel conductance of 26.9 ± 0.8 pS (n = 5). The other type was highly Na+ selective (i.e. Na+ channel) and had an inwardly rectifying I/V relationship with a single-channel conductance of 11.8 ± 0.2 pS (n = 5) around resting membrane potential. The NSC channel was more frequently observed (1.37 ± 0.15 per patch membrane; n = 73) than the Na+ channel (0.15 ± 0.40 per patch membrane; n = 73). However, the open probability of the NSC channel was smaller than that of the Na+ channel. Both types of the channels were activated by cytosolic Ca2+, however the sensitivity to cytosolic Ca2+ was much higher in the Na+ channel than in the NSC channel. Furthermore, both types of the channels were blocked by amiloride or benzamil. The half-maximal inhibitory concentration (IC50) of amiloride or benzamil of the Na+ channel was 1–2 μM, while that of NSC channel was less than 1 μM. Both channels were activated by insulin.
    Materialart: Digitale Medien
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  • 20
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 58 (1996), S. 707-715 
    ISSN: 0020-7608
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A series of different isodesmic and homodesmic reactions defining strain energies in 3-membered rings are described and discussed. One isodesmic and one homodesmic reaction are applied numerically with the purpose of estimating strain in heterosiliranes including second-row and third-row heteroatoms. All molecules involved are optimized using SCF/6-31G**, and energies are calculated using MP2/6-31G**//SCF/6-31G** calculations. The results are discussed with reference to limitations of the chosen models. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 6 Tab.
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  • 21
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996) 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 22
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 539-544 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The oxidation of ethylbenzene with Ph4PHSO5 catalyzed by Mn(TMP)Cl in the presence of 4-tert-butylpyridine was studied in 1,2-dichloroethane. The reaction affords acetophenone together with minor amounts of 1-phenylethyl alcohol. The oxidation of 1-phenylethyl alcohol to acetophenone was studied under identical experimental conditions. In both cases, the oxidation rates are independent of the concentration of the substrates whereas they depend linearly on catalyst concentration. By increasing the concentration of 4-tert-butylpyridine, which acts as an axial ligand of the catalyst, saturation behavior is observed. The observations reported above, together with the chemoselectivity observed, the fact that the reactivities of the alkane and of the alcohol are similar and the activation parameters of ethylbenzene oxidation (ΔH
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 23
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 588-591 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: When 2-(tert-alkyl)adamantan-2-ols (where the substituent is bi- or tricyclic) are thermolysed or the corresponding bromide is refluxed in pyridine, an unusual 1,3-elimination occurs, leading to 2,4-dehydroadamantanes bearing the tert-alkyl substituent on the cyclopropane system.
    Materialart: Digitale Medien
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  • 24
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 593-597 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A study of the acid-base behaviour of the three isomeric pyridinecarboxylic acids (picolinic, nicotinic and isonicotinic acid) was carried out using spectrophotometric and potentiometric measurements. The cationic form of picolinic acid converts partially into the corresponding zwitterion (pK1) within a borderline acidity range where neither the pH scale nor the acidity functions work satisfactorily. Protonation of the carboxyl groups (pK33) occurred at the highest acidity levels employed. The medium effects observed on the spectral curves were corrected by factor analysis. The potentiometric measurements gave values for pK1 and pK2 only, which were in good agreement with those determined spectrophotometrically.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 25
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Cyclic voltammetry of 1-nitroso-2-naphthol in the potential region 0 to 1·0 V vs Ag/AgCl using glassy carbon and platinum electrodes shows a reversible redox couple. The electrode process is diffusion controlled and corresponds to an EC mechanism. The one-electron oxidation product, an iminoxyl radical, is characterized by a triplet ESR signal at g = 2·0067 further split by three ring hydrogens. This radical is unusually long-lived, with half-life times of 150 s in water and 3600 s in acetonitrile.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 26
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Kinetic studies were carried out on the reactions of anilines with 2-cyano-2-propyl and 1-cyanocyclooctyl arenesulfonates in acetonitrile at 50·0°C. The second-order rate constants for the former are in general greater than those for the latter but the rates of the two become comparable for a strong nucleofuge. The cross-interaction constants, ρXZ (and βXZ), are considerably smaller (ca -0·04) than those for the primary (ca 0·33) and secondary (ca 0·12) compounds. The negative sign and small magnitude are consistent with a dissociative SN2 mechanism with a loose transition state structure. The ab initio MO theoretical results for Cl- + RCl ClR + Cl- at the MP2 level (MP2/6-31 + G*//MP2/6-31 + G*) confirm the looseness of the transition state for the tertiary (R) alkyl compounds. The average r(Cl…Cl) value is 47middot;88 ± 0·03 Å, which is larger than those for the reactions at primary (4·68 ± 0·02 Å) and secondary (4·80 ± 07middot;02 Å) carbon centers. Thus a looser transition state with a smaller magnitude of ρXZ for the tertiary carbon centers has a larger theoretical r(Cl…Cl) value.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 27
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A 1H NMR conformational study of cis- and trans-4-substituted cyclohexene oxides revealed an increased predominance, as compared with the parent 4-substituted cyclohexenes, of the equatorial conformer for cis-isomers and a preference of the axial conformer for trans-isomers. These conformational shifts can be rationalized in terms of intramolecular dipole-dipole and/or steric interactions. However, molecular mechanics calculations failed to reproduce the relative stability of the axial conformer in trans-4-substituted cyclohexene oxides.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 28
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996) 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 29
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 711-716 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Reaction pathways leading to nucleophilic addition and enolate formation were investigated for the reaction between acetaldehyde and hydroxide anion. Ab initio calculations predict small activation barriers for both reactions in the gas phase. Monte Carlo simulations were performed to assess the effects of aqueous solvation. It was found that both reaction pathways involve significant solvent-induced activation barriers, in addition to effecting some structural changes in the transition state.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 30
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 770-776 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The reactions of O-(2,4-dinitrophenyl)-substituted p,p′-dimethoxybenzophenone oxime, p,p′-fluorobenzophenone oxime and p,p′-dichlorobenzophenone oxime with pyrrolidine and piperidine in benzene were found to be third order in amine, with no uncatalytic route. The overall rate is a combined effect of rates of two routes, one of which increases and the other decreases with rise in temperature. The relative contribution of the two routes to overall rate varies with temperature, nucleofugicity of the substrate, nucleophilicity and concentration of amine. As a result, the effect of temperature on the overall rate for some reactions is positive and for others negative. This unusual temperature effect on the overall rate supports Hirst's mechanism.
    Zusätzliches Material: 5 Ill.
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  • 31
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 751-758 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Absolute rate studies were carried out on a series of C(SINGLE BOND)H insertion reactions of dimethyldioxirane (1a). The substrates were chosen so that the distance between a single tertiary C(SINGLE BOND)H bond and an OH group could be varied. The measured rate constants indicate that a rate acceleration occurs when the distance between the reacting C(SINGLE BOND)H bond and the OH group permits intramolecular H-bonding stabilization of the transition state. A similar study in related compounds without the OH group showed no effect of chain length on the rate of the C(SINGLE BOND)H insertion reaction. A related study of the epoxidation reaction of la also found an increased rate when chain length permitted intramolecular H-bonding by an OH group.
    Zusätzliches Material: 5 Tab.
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  • 32
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996) 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 33
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 746-750 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The 15N NMR chemical shifts of eight substituted pyridine N-oxides (B) and their complexes (AHB) with methanol and dichloroacetic and trifluoromethanesulfonic acids were measured in chloroform-d at the natural abundance level. The measured chemical shifts are strongly affected by substituents, hydrogen bond strength and protonation. The plot of the relative chemical shifts, Δδ(15N) = δ(AHB) - δ(B), against ΔpKa gives a titration curve that reflects the variation of the hydrogen bond strength and the proton moves from the acid to the N-oxide. According to previous IR data, in the complexes from the inversion region (ΔpKa = 1·26), the proton is either delocalized (B…H…A) or more likely the lifetime is so short (≤10-13 s) that the method does not recognize the B…H-A and B+H…A- species. Protonation of pyridine N-oxides shifts the nitrogen signal ca 50 ppm to lower frequencies compared with the ca 123 ppm for pyridines.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 34
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 781-786 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 13C and 15N NMR data are reported for two substituted nitronaphthalenes 1,8-bis(4-toluenesulphonamido)-2,4,7-trinitronaphthalene and 1,8-bis(4-toluenesulphonamido)-2,4,5,7-tetranitronaphthalene and their salts with 1,8-dimethylaminonaphthalene. The salts are shown to contain NHN+ and NHN- intramolecular hydrogen-bonded systems in CD3CN solutions, in agreement with x-ray diffraction data on solid samples and 1H NMR studies on solutions. Examples are given of both a symmetrical and an unsymmetrical bonding system for the NHN atoms. 15N NMR is shown to be particularly helpful in these studies, both 15N shielding and 1J(15N, 1H) couplings are of value. Additional assistance is obtained from 3J(13C9, N1H) data. © 1996 John Wiley & Sons, Ltd.
    Zusätzliches Material: 1 Ill.
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  • 35
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 787-794 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The kinetics of the gas-phase elimination of three 2-alkoxyacetic acids were investigated in a static system, seasoned with allyl bromide, and in the presence of the free chain radical inhibitor cyclohexene. The working temperature and pressure range were 350·4-410·8°C and 57-261·5 torr, respectively. The reactions proved to be homogeneous and unimolecular and to follow a first-order rate law. The temperature dependence of the rate coefficients is given by the following equations: for 2-methoxyacetic acid, log k1 (s-1) = (12·10 ± 0·22)-(193·3 ± 2·8) kJ mol-1 (2·303RT)-1; for 2-ethoxyacetic acid, log k1 (s-1) = (12·76 ± 0·29)-(199·6 ± 3·7) kJ mol-1 (2·303RT)-1; and for 2-isopropoxyacetic acid, log k1 (s-1) = (12·40 ± 0·32)-(193·7 ± 3·9) kJ mol-1 (2·303RT)-1. The alkyl group R in ROCH2COOH does not seem to exert a significant effect on the rates. It is postulated that the predominant mechanism for the decomposition of the alkoxy acids involves a five-membered cyclic transition state, where the elimination of the RO substituents is assisted by the acidic proton of the COOH group. © 1996 John Wiley & Sons, Ltd.
    Zusätzliches Material: 8 Tab.
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  • 36
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 801-810 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The potential energy surface for the thermal isomerization of fulvene to benzene was studied by modified Gaussian-2 (G2M) and the bond additivity-corrected fourth-order perturbation Møller-Plesset (BAC-MP4) methods. Three isomerization pathways were investigated. One involves the intermediate prefulvene by a concerted mechanism, which has a significantly higher barrier. The second, also involving prefulvene and cyclopenta-1,3-dienylcarbene intermediates, has a barrier of 84·0 kcal mol-1. The third, a multi-step pathway, includes bicyclo[3.1.0]hexa-1,3-diene and cyclohexadiene carbene intermediates. The activation energy of the multi-step pathway was calculated to be 74·3 kcal mol-1, which is 7-11 kcal mol-1 higher than the experimental value obtained by a brief very low-pressure pyrolysis (VLPP) study. RRKM calculations were performed on the multi-step pathway in order to determine the rate of isomerization. These theoretical results cast doubt on the validity of the VLPP data. © 1996 John Wiley & Sons, Ltd.
    Zusätzliches Material: 4 Ill.
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  • 37
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996) 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 38
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 795-800 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The enantioselective solid-solid clathration of (S)-pantolactone (1) into (R,R)-trans-2,3-bis(diphenylhydroxymethyl)-1,4-dioxaspiro[4·4]nonane (2) and -[4·5]decane (3) was studied preparatively and mechanistically using atomic force microscopy (AFM) measurements and crystal packing data. Short-distance solid-to-solid sublimation mechanisms occur in both cases with initial formation of epitaxial floes along the b-axis in 2 and random craters in 3. The bulk control in the phase rebuilding stage is understood from the particular crystal packings. Bulk control was largely lost in the phase transformation stage when passivation of the surfaces occurred in both cases. The host lattices of 2 and 3 exhibit closed molecular double layers with all hydroxyl groups inside and lacking access for intercalation of 1. The reaction has to start at isolated surface defects. Once started, new doors for further entrance of guest molecules (S)-1 are opened in the double layer. For practical use, both the crystallographic difficulties and the passivation have to be overcome. A slurry technique involving addition of stoichiometric amounts of water to the solids provided useful conditions for the preparative resolution of (R/S)-1 or further racemates exhibiting passivation, whereas heating alone speeded up the resolution of 2-methylpiperazine with 2. © 1996 John Wiley & Sons, Ltd.
    Zusätzliches Material: 2 Ill.
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  • 39
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 119-127 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The conformational space of the 2-cyano-1,1-dihydroxyethane molecule was studied at the semi-empirical PM3 level and ab initio MP2/6-31G**//6-31G level in the gas phase and in a low-polarity medium. This system has been chosen as a model compound for 2-cyanocyclohexanone propylene and ethylene acetals. This has allowed the study of the role of polar groups on the relative conformation of two adjacent OH groups, which is of interest also in relation to the anomeric effect in carbohydrate chemistry. Solvent effects are taken into account using a continuum model with general cavity shapes.
    Zusätzliches Material: 3 Ill.
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  • 40
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996) 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 41
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 111-118 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A spectrofluorimetric titration analysis of the proton dissociation and the interactions of human serum transferrin with hydrogencarbonate was performed at pH 7·0-9·0. Apotransferrin loses a single proton probably per binding site with Ka = (6·80 ± 0·35) × 10-9 M. This proton dissociation is independent of the hydrogencarbonate concentration. Apotransferrin does not interact with CO32-. However, it interacts with two HCO3-, exhibiting two different affinity constants; the dissociation constant presumably for the C-site is KC = (4·40 ± 0·15) × 10-3 M and that for presumably the N-site is KN = (3·60 ± 0·30) × 10-2 M. These interactions are independent of pH and occur with the unprotonated and protonated apotransferrin species with the same low affinities. Such affinities are probably induced by ionic interactions involving the side chain of the arginine residues in each of the two binding sites. As for the proton dissociation, it can occur with one of the other side-chains of the amino acid residues of these binding sites.
    Zusätzliches Material: 8 Ill.
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  • 42
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 159-167 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The structures of several sulfoxides, including dimethyl sulfoxide and pentamethylene sulfoxide, were fitted with the MM3 force field to existing experimental data from electron diffraction and microwave spectroscopy. The vibrational spectra were also fitted for dimethyl sulfoxide. The torsional parameters could not be determined from existing experimental data, so the torsional profile for methyl ethyl sulfoxide was fitted to ab initio values.
    Zusätzliches Material: 1 Ill.
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  • 43
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 129-136 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Previously unknown 1,3-dioxenium perchlorates were obtained by coupling 1,3-diketones with aliphatic ketones in an acetic acid solution of perchloric acid. The dioxenium ring of 4,6-bis(p-methoxystyryl)-2,2-pentamethylenespiro-1,3-dioxenium perchlorate in the crystal possesses the envelope conformation, the geometry of the carbon triad being close to that of the allyl cations. Variable-temperature 1H NMR spectra of unsymmetrical 1,3-dioxenium cations revealed the occurrence of a sufficiently fast enantiotopomerization process governed by the C(SINGLE BOND)O bond dissociation-recombination mechanism.
    Zusätzliches Material: 4 Ill.
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  • 44
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 145-151 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Second-order rate constants of reactions of HO- with phosphate, phosphinate and thiophosphinate esters, (PhO)2PO.OC6H4NO2-p, Ph2PO.OC6H4NO2-p, Ph2PO.SPh, Ph2PO.SC6H4NO2-p and Ph2PO.SEt, go through minima with decreasing water content of H2O-MeCN or H2O-t-BuOH. The rate decrease is due to stabilization of the non-ionic ester on addition of organic solvent to H2O. This inhibition is partially offset by stabilization of the anionic transition states and in the drier solvents partial desolvation of HO- increases rates.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 45
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Reactions of morpholine in dimethyl sulphoxide at unsubstituted ring positions of 1,3,5-trinitrobenzene, and phenyl 2,4,6-trinitrophenyl ether, yield anionic σ-adducts via zwitterionic intermediates. Reactions at the 1-position of phenyl 2,4,6-trinitrophenyl ether, phenyl 2,4-dinitronaphthyl ether, and phenyl 2,4-dinitrophenyl ether result in substitution of the phenoxy groups. In both these reaction types proton-transfer is rate-limiting. Comparison of kinetic and equilibrium data with those for corresponding reactions of piperidine shows that rate constants for proton transfer are similar for the two amines, but equilibrium constants for zwitterion formation have lower values for morpholine, the less basic amine. Implications for base catalysis are discussed.
    Zusätzliches Material: 3 Ill.
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  • 46
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 191-202 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The MM3 force field has been extended to include the nitriles and alkynes. Structures, heats of formation, dipole moments and conformational equilibria for aliphatic nitriles and alkynes compounds are fitted to within experimental error. The vibrational spectra for aliphatic nitriles and alkynes were studied, and the experimental values were fitted to an rms error of about 30 cm-1. Previous MM2 studies of nitriles and alkynes left unresolved the length of the Csp(SINGLE BOND)Csp3 bonds in isopropylnitrile, 3-methylbutyne, and tert-butylacetylene. In each of these compounds, previous MM2 results disagree with experiment. The present MM3 studies and quantum mechanical calculations (MP2/6-31G** and B3LYP/6-31G*) confirmed the previous MM2 results.
    Zusätzliches Material: 10 Tab.
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  • 47
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 227-233 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The diazotization of N-silylated N-methyl- and N-phenylcyclopentenylamines affords products derived from intermediate methyl- and phenyldiazonium ions. However, when this method is applied to N,N-bissilylated cyclopentenylamines, the products obtained do not confirm the formation of a cyclopentenyl cation intermediate.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 48
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 203-211 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A theoretical and experimental analysis of the geometric and electronic properties of compounds containing the aminosulphonylamino moiety was carried out. The theoretical properties were calculated using molecular orbital ab initio methods at the Hartree-Fock (HF) and second order Möller-Plesset (MP2) levels of theory, local density functional (LDF) ab initio methods and the semi-ab initio method, SAM1, on sulphamide and seven heterocyclic compounds containing the aminosulphonylamino group. The experimental analysis has been performed using x-ray structures of related compounds gathered in the Cambridge Structural Database together with experimental dipole moments and 13CNMR shifts of some of the compounds studied. Comparison of the experimental analysis with the theoretical results indicates that none of the methods studied is the most adequate to describe the geometry and electronic distribution of these molecules. The use of the 6-31G* basis set to compute the geometry of these molecules and methods which include electronic correlation (MP2/61G*//RHF/6-31G*, MP2/6-31G* and LDF) to quantify their electronic distribution are proposed.
    Zusätzliches Material: 1 Ill.
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  • 49
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Upon irradiation, 2-(dibenzylamino)ethyl and 2-(N-benzyl-N-methylamino)ethyl acetoacetate (1a and 1b) undergo photocyclization via remote proton transfer from the benzyl group to the acetyl carbonyl oxygen to give eight-membered azalactones. Irradiation of the corresponding (diisopropylamino)- and (dimethylamino)ethyl esters gave no azalactones. Introduction of the methyl group on C-2 of 1a brought about a complicated photoreaction, probably due to competition of α-cleavage. The Stern-Volmer plots for the photoreaction of 1a did not show the linear relationship, indicating that the photoreaction proceeds from two reactive excited states. The Stern-Volmer quenching equation for the system was obtained by applying the steady-state approximation and was used for the analysis of the photoreaction of 1a. The triplet lifetime was determined to be 1·6 × 10-8 s.
    Zusätzliches Material: 4 Ill.
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  • 50
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In order to extend the the method for preparation of amidines using N-Mg reagents, aryl- and alkyliminodimagnesium [IDMg, ArN(MgBr)2 and RN(MgBr)2] were reacted with esters, amides, ortho- esters, acetals, aminoacetal and arene- and alkane carbonitriles. Among the compounds used, aminoacetal and carbonitriles were proved to be useful as starting materials for amidine preparation; alkyl-IDMgs were successfully used for the first time. It was noted that an excess molar amount of IDMg is needed in the reported reaction of ArN(MgBr)2 with benzonitrile (aryl-aryl combination), whereas no excess is needed in aryl-alkyl, alkyl-aryl, and alkyl-alkyl combinations of reagent and substrate. From the viewpoint previously proposed in terms of relative efficiency of single electron transfer in the reactions of magnesium reagents, the most probable reason for the difference in the need for an excess molar amount of aryl and alkyl IDMg was ascribed to the difference in the electron-donating abilities of reagents. Additional minor reasons are discussed.
    Zusätzliches Material: 1 Ill.
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  • 51
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996) 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 52
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 234-240 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Information on the rotational motion of various types of spin-labelled long-chain nitroxides was obtained from the anisotropic ESR signals. By varying the position of the nitroxide moiety along the chain, the intrinsic flexibility of molecular chain was examined. The rotational correlation times (τc) of spin-labelled long-chain nitroxides were about 10-10 s. The activation parameters for rotational motion were estimated from the temperature and pressure dependences of τc. It was found that the activation entropy observed for methyl 16-doxyl stearate is obviously large compared with those for methyl 5- and methyl 12-doxyl stearates. The results suggest an increase in the molecular motions at the end of the hydrocarbon chain. The viscosity dependence of τc is discussed in terms of the difference in the strength between solute-solvent and solvent-solvent interactions.
    Zusätzliches Material: 3 Ill.
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  • 53
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 295-300 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The ionized (S-) and non-ionized (SH) phenyl (PSH) and methyl (MSH) salicylates exhibit strong and undetectable absorption at 350 nm, respectively. These molecular absorption properties were used to determine the binding constants of S- and SH with the micelles of sodium dodecyl sulphate in terms of the pseudophase model of micelles. The binding constants (K1) of S- are 4·0 ± 2·0 dm3 mol-1 for PSH and 5·7 ± 1·2 dm3 mol-1 for MSH and those (K2) of SH are 2350 ± 90 dm3 mol-1 for PSH and 100 ± 10 dm3 mol-1 for MSH at 30°C.
    Zusätzliches Material: 2 Ill.
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  • 54
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 279-286 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The kinetics of the oxidation of six substituted phenethyl alcohols by sodium N-chlorobenzenesulphonamide or chloramine-B (CAB) in the presence of HCl was studied at 35°C. The rate shows a first order dependence on [CAB]0 and [H+] and is of fractional order in [PEA]0 and [Cl-]. Ionic strength variations, addition of the reaction product of benzenesulphonamide and variation of the dielectric constant of the medium have no effect on the rate. The solvent isotope effect k1H2O/k1D2O ≅ 0·78. Proton inventory studies were made in H2O-D2O mixtures. The rates correlate satisfactorily with Hammett's LFER. The reaction constant ρ was -3·5 for electron-releasing substituents and -0·30 for electron withdrawing groups at 35°C. Activation parameters ΔH
    Zusätzliches Material: 7 Ill.
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  • 55
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 255-261 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Measurements were made in CCl4 of the formation constant KHB of the 1:1 hydrogen-bonded complexes between the reference donor 4-fluorophenol and the intramolecular hydrogen-bonded systems I (one lone pair on heteroatom Y, one intramolecular hydrogen bond: 8-hydroxyquinaldine and 2-(2-hydroxyphenyl)benzoxazole); II: (two lone pairs, two intramolecular hydrogen bonds: 2,2′-dihydroxybenzophenone and 1,8-dihydroxyanthrone) and III (two lone pairs, one intramolecular hydrogen bond: tropolone, salicylic acid derivatives and guaiacol). The pKHB values and the structural vibrational studies show that system I has a non-zero hydrogen-bond basicity which is due to the oxygen atom. In system II the non-zero basicity is explained by the two oxygens and the breaking of one intramolecular hydrogen bond. In the push-pull system III (e.g. tropolone), in spite of the great decrease of the basicity of the free lone pair by the intramolecular hydrogen bond (e.g. compared with tropone), Y remains the major site for intermolecular association. However in guaiacol, a non push-pull system III, the cooperativity effect makes the phenolic oxygen the major site.
    Zusätzliches Material: 3 Ill.
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  • 56
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 262-264 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: From a set of photochromic spiro[indoline-naphthoxazines] substituted on the oxazine part, a correlation between the electronic charge of the 2′-carbon atom and the absorption wavenumbers of the corresponding coloured forms was found. This relationship is of particular interest to predict the colour developed by this class of photochromic compounds.
    Zusätzliches Material: 2 Ill.
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  • 57
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 265-268 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The acid-base properties of eight 3-aminopropionamidine derivatives R1R2N(CH2)2C((DOUBLE BOND)NH)NR3R4 (1, R1 = R2 = R3 = R4 = H; 2, R1 = R3 = R4 = H, R2 = Me; 3, R1 = R2 = R4 = H, R3 = Me; 4, R1 = R2 = H, R3 = R4 = Me; 5, R1 = Tos, R2 = R3 = R4 = H; 6, R1 = Tos, R2 = Me R3 = R4 = H; 7, R1 = Tos, R2 = R4 = H, R3 = Me; 8, R1 = Tos, R2 = H, R3 = R4 = Me; Tos = 4-toluenesulphonyl) related to the antiviral natural product distamycin A were investigated in water and dimethyl sulphoxide (DMSO). The measured pKa values for the ammonium function in 1-4 in water ranged between 7·48 and 7·73, whereas the corresponding values in DMSO were 9·4 ± 0·3. The amidinium moiety of these compounds displayed pKa values in the range 11·4-12·0 and 13·4-13·6 in water and DMSO, respectively. The tosylamide group in compounds 5-8 was deprotonated in the expected pH region and exhibited pKa values between 9·49 and 10·02 in water, but was considerably less acidic in DMSO (14·5 ≤ pKa ≤ 15·7). The behaviour of the amidinium cation of 5-8 in water and DMSO resembled that of 1-4. The measured pKa values are discussed and the solvent-induced pKa shifts are explained in terms of solvent and substituent effects. The observed pKa differences between the ammonium and the amidinium functions in 1-4 render these compounds suitable intermediates in an alternative synthesis of distamycin A.
    Zusätzliches Material: 1 Ill.
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  • 58
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 252-254 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: It is reported that earlier assignments of 2-naphthylphenylcarbene were erroneous and that ESR data support the same assignment as quantum mechanical calculations. An unambiguous nomenclature for geometric isomers of carbenes is proposed.
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  • 59
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 241-251 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The known correlations between calorimetric and IR spectroscopic data on hydrogen bonding were reinvestigated for hydrogen bond donors (AH) dissolved in pure bases (B). Ninety-five AH···B systems were considered for which the enthalpies of specific interaction due to hydrogen bonding AH···B (ΔHAH/Bsp.int., kJ mol-1), the weight centers of A-H stretching bands (v, cm-1) and their integral absorption coefficients (α, 104 cm mmol-1) had been measured. The relationships between ΔHAH/Bsp.int. and the parameters of the infrared absorption spectra [weight center shifts Δv and the changes in the square roots of α (Δα1/2)] were analyzed. It was found that the dependence of ΔHAH/Bsp.int. on Δα1/2 consists of two nearly parallel straight lines: the first (-ΔHAH/Bsp.int. = 12·0 Δα1/2 + 0·4) corresponds to water and the weak C(SINGLE BOND)H and O(SINGLE BOND)H H-bond donors (chloroethylenes, acetylenes acetonitrile, nitromethane, chloroform, o, o′-di-tert-butylphenol); the second (-ΔHAH/Bsp.int. = 12·1 Δα1/2 -4·2) corresponds to the stronger N(SINGLE BOND)H and O(SINGLE BOND)H H-bond donors (N-methylaniline, pyrrole, alcohols, phenol, carbon acids). Non-linear dependences of ΔHAH/Bsp.int. on Δv were obtained for all C(SINGLE BOND)H, N(SINGLE BOND)H and O(SINGLE BOND)H H-bond donors except water [-ΔHAH/Bsp.int. = 59·9 Δv/(Δv + 674)]. Enthalpies of specific interaction for water obey another dependence [-ΔHH2O/Bsp.int./2 = 28·5 Δv/(Δv + 269)]. The ΔHAH/Bsp.int. values can be estimated by the above correlations with an accuracy of ±3 to ±6 kJ mol-1. These relationships obtained for solutions of H-bond donors in pure bases differ from the well known dependences determined for the AH···B hydrogen bonding in carbon tetrachloride medium.
    Zusätzliches Material: 5 Ill.
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  • 60
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 487-497 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: An experimental and theoretical study of the structure and aggregation of diphenylguanidine (DPhG) in non-polar and low-polarity solvents (CCl4, C6H6, C2HCl3 and CHCl3) was performed. Dipole moments, IR spectra and average molecular weight measurements as a function of concentration demonstrate that DPhG is strongly associated in the solvents studied. The dimerization constant in CCl4 is 192 ± 7 dm3mol-1. Experimental results and a theoretical discussion on the basis of MNDO-PM3 and -AM1 methods show that in low-polarity solvents DPhG exists in the form of an asymmetric tautomer, the same as was found in the solid-state structure.
    Zusätzliches Material: 10 Ill.
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  • 61
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The kinetics of the reaction between 1-chloro-2,4-dinitrobenzene and piperidine was studied in several completely non-aqueous binary solvent mixtures where the preferential solvation is the rule at 15, 25 and 40°C. The reaction was chosen as the simplest example of aromatic nucleophilic substitutions (ANS). For (aprotic solvent + aprotic co-solvent) binary systems the co-solvent was toluene, and the rest of the solvents used were selected with different structural characteristics and an extensive range of polarity. In this kind of mixture a property of mixed binary solvents would be defined by means of ET(30) values and the solvent effects on this simple model of ANS reactions are similar to those of aprotic pure solvents, especially if hydrogen-bond donor solvent mixtures are excluded from the analysis. For (aprotic solvent + protic co-solvent) binary systems the co-solvent used was methanol. The presence of a protic solvent in the mixture strongly determines the solvent effects on the reaction. In this type of binary mixture, the chemical probe under consideration may not be generally valid to interpret solvation effects. Additionally, empirical solvent polarity parameters ET(30) were determined UV-VIS spectrophotometrically for some pure aprotic solvents and, as a function of the composition, for (dimethylformamide + toluene), (toluene + methanol) and (1,1,1-trichloroethane + methanol) at 15 and 40°C, with the purpose of extending the studies on the empirical polarity indices in binary solvent mixtures to the thermo-solvatochromic area.
    Zusätzliches Material: 6 Ill.
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  • 62
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A theoretical study of the catalytic mechanism of lactate dehydrogenase enzyme on different model systems was carried out with the help of the PM3 semi-empirical procedure and an ab initio method at the 4-31G and 6-31G** basis sets at a Hartree-Fock (HF) level of theory.The geometry, transition vector (TV) and electronic structure of the transition structure (TS) for the acid-catalysed hydride reduction were obtained. The dependence of these properties on the computing method and model system is analysed and discussed. Proton transfer is much more advanced than hydride transfer occurring in roughly perpendicular planes. All the TSs render very similar structural features, the control of the chemical reaction being associated with the hydride transfer process. A comparison among simple and sophisticated molecular models shows that the TS seems to be structurally a rather robust entity. There is a minimal molecular model with a TS which describes the essentials of the chemical interconversion step in a given enzyme mechanism and the corresponding TV is an invariant feature.
    Zusätzliches Material: 11 Ill.
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  • 63
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 507-513 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Adamantane and 1,3,5,7-tetradeuterioadamantane were oxidized by RuO4 in two solvent systems, CCl4-CH3CN-H2O and acetone-water, yielding two kinetic deuterium isotope effects (KIEs), 4·8 ± 0·2 and 7·8 ± 0·1, respectively, very similar to those obtained in analogous reactions with cis-decalin and perdeuterio-cis-decalin, 4·8 and 6·8. These results were interpreted as primary KIEs and small or negligible secondary KIEs. From this, sp2-hybridized intermediates were not involved in the reaction path. The kinetic effect of the solvent was investigated by performing the reaction in aqueous acetone and acetonitrile. The rates were correlated with Grunwald-Winstein Y values and with Reichardt ET (30) values. Both correlations showed the reaction to be only moderately dependent on the solvent polarity. 1-Substituted adamantanes were oxidized in CCl4-CH3CN giving a Taft ρ* value of -2·5 ± 0·1. These results were regarded as support for a reaction consisting of a pre-equilibrium with formation of a substrate-RuO4 complex followed by a rate-determining concerted reaction. The results did not support a reaction mechanism with a carbocation or radical intermediate, or a scheme with two competing reactions, one with a carbocation intermediate and the other with a concerted mechanism.
    Zusätzliches Material: 2 Ill.
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  • 64
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The product ion distributions and rates of the gas-phase reactions of two series of (radical) anions with chloro- and bromomethanes (CH3Cl, CH2Cl2, CHCl3, CCl4, CH3Br, CH2Br2, CHBr3 and CBr4) were determined with the use of Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry. The first series consists of anions (HO-, CH3O-, C2H5O-, C3H7O- and CH3S-), for which the corresponding neutral radicals have a relatively high electron affinity (EA 〉 150 kJ mol-1). The second series consists of (radical) anions (CH2S-·, CH2(DOUBLE BOND)CHCH2-, CH2(DOUBLE BOND)C(CH3)CH2-, C6H4-· and C6H5-), for which the corresponding neutral species have a relatively low electron affinity (EA ≤ 100 kJ mol-1). These (radical) anions react mainly with the halomethanes to afford (i) halide ions, (ii) halomethyl anions with the same number of halogen atoms as in the parent halomethane and (iii) halomethyl anions with one halogen atom less than the parent substrate. The last process involves nucleophilic attack on a halogen atom and is particularly important in the reactions with substrates containing three or four halogen atoms. The halide ions may arise by a number of different pathways, such as SN2 substitution, α-elimination, halogen attack followed by dissociation of the thus formed halomethyl anion and overall dissociative electron transfer. The SN2 process is held responsible for the formation of halide ions in the reactions with monohalomethanes, whereas α-elimination is likely to be of importance only for the reactions with trichloro- and tribromomethanes. Attack on a halogen atom followed by dissociation of the ion generated initially is likely to be important if CCl4 or CBr4 is the substrate. Electron transfer is only a dominant pathway in the reactions of the CH2S-· ion with the halomethanes. The occurrence of electron transfer in the reactions of this ion with CHCl3, CCl4 and CHBr3 is evidenced by the formation of minor amounts of stable halomethane radical anions in addition to the generation of CH2SCl- or CH2SBr- ions and abundant halide ions. The interplay between the various possible reactions is discussed on the basis of thermodynamic considerations and the rates of the overall processes.
    Zusätzliches Material: 5 Ill.
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  • 65
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 759-769 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Rate constants of reaction of cyclopentadienylidene, fluorenylidene and tetrachlorocyclopentadienylidene with alcohols and other quenchers were determined by laser flash photolysis methods. The rate constants of reaction of cyclopentadienylidene and fluorenylidene with various alcohols were determined and found to increase with increasing alcohol acidity. Alcohols as a group reacted faster with cyclopentadienylidene and fluorenylidene than likely ylide formers such as pyridine, ethyl acetate and tetrahydrofuran. Brønsted plots of the reaction of cyclopentadienylidene and fluorenylidene with alcohols are linear with slopes of 0·061 and 0·082, respectively. In the case of tetrachlorocyclopentadienylidene, an ylide type of reaction mechanism with alcohols is indicated. Tetrachlorocyclopentadienylidene reacts most rapidly with the least acidic alcohol studied and this carbene reacts more rapidly with tetramethylurea, pyridine and tetrahydrofuran than with methanol.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
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  • 66
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 739-745 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The x-ray molecular structures of five chiral phosphoramidates derived from N-phosphorylated nitrogen mustard were determined and the molecular parameters are discussed. The value of the torsion angle of the O(SINGLE BOND)P(SINGLE BOND)N(SINGLE BOND)H function which determines the packing of the molecules was found to determine also the ability of a substrate to form diastereomeric hydrogen-bonded complexes with optically active acids.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 67
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 729-738 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A qualitative analysis is presented of the interrelationships between phase transformations and organic chemical reactivity in the solid state, taking into consideration general thermochemical relationships and the thermodynamics of heterophase equilibrium. Two cases, where isomerization reactions depend on the solid-state solubility of the reactant and product, are considered and show that the formation of a new phase can influence both the reaction yield and rate. For example, it is shown that crystallization of a new phase from a crystalline or amorphous solid solution can supply the thermodynamic driving force for chemical transformation. Formation of a new phase may influence solid-state kinetics depending on the solubility of a reactant in the new phase and the relative rates of chemical transformation and formation of the new phase. It is further shown that even for simple monomolecular reactions, kinetic curves for the overall process can consist of up to five parts, depending on the type of phase diagram involved. These principles have been applied to some examples of solid-state isomerization in a way that allows the choice of a proper kinetic scheme and an explanation of the direction and maximum yield observed for a particular reaction.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 68
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Evaluation of the rates of solvolysis of 2-chloro-2,4,4-trimethylpentane (4) in 17 solvents on the basis of the Grunwald-Winstein type equation [log(k/k0) = lNT + mYCl + c] gives an excellent correlation with l = -0·01 ± 0·02 and m = 0·74 ± 0·01. The neopentyl group in 4 more effectively shields the rear side of the reaction center than the tert-butyl group in 2-chloro-2,3,3-trimethylbutane. The rate ratio between 4 and 2-chloro-2-methylpropane (3) at 25°C is 275 in trifluoroethanol and predicted to increase to 950 in trifluoroacetic acid. The previous 4:3 rate ratio of 22 in 80% ethanol evidently underestimated the B-strain effect on the solvolysis rate of 4 by a factor of at least 40.
    Zusätzliches Material: 2 Ill.
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  • 69
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 1-6 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Reaction of (Z)-[6]paracycloph-3-ene (2) with tetracyanoethylene (TCNE) gave a [2 + 2] cycloadduct (4), which represents the first example of thermal [2 + 2] cycloaddition of a benzene derivative under mild conditions. The structure of 4 was confirmed by x-ray crystallographic analysis. Semi-empirical PM3 calculations and the measurement of the He I photoelectron spectrum of 2 indicated that the ionization potential of 2 is considerably lower than that of [6]paracyclophane (1), which gave a [4 + 2] cycloadduct (3) with TCNE. The unusual pericyclic selectivity and regioselectivity are discussed on the basis of PM3 calculations. The regioselectivity is ascribed to the higher φ bond order of the bridgehead aromatic bond of 2, which is on the same side of the bridge double bond, than that of the bond on the opposite side of the bridge double bond.
    Zusätzliches Material: 2 Ill.
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  • 70
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 17-20 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In a recent paper [N.S. Isaacs and A. Laila, J. Phys. Org. Chem. 7, 178 (1994)2] the volume profile for the cheletropic addition of sulphur dioxide to a 1,3-diene (2,3-dimethylbuta-1,3-diene) indicated that a two-step mechanism for this reaction, with a (4 + 2) cycloaddition at the S(DOUBLE BOND)O bond as the slow step followed by a rapid rearrangement of the resultant sulpheno-lactone, cannot be ruled out. However, ab initio calculations, at the MP2(FC)/6-31G*//RHF/6-31G* level, show that such a mechanism can be conclusively discarded.
    Zusätzliches Material: 1 Ill.
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  • 71
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 7-16 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A series of tetracoordinated boron complexes derived from various 1,3-diketones and bidentate ligands (oxalato, malonato, catecholato and difluoro) were prepared. Their absorption, fluorescence and phosphorescence spectra, at ambient temperature and 77 K, and cyclic voltammmetry in acetonitrile were studied. The boron complexes exhibited high molar absorptivity and fluorescence intensities as compared with the parent diketones; the phenomena are in agreement with the lowest singlet excited state possessing the φ, φ,* configuration with a rigid chelate structure. The redox potential differences correlate linearly with the lowest singlet (Es) as well as the triplet (ET) excited state energy with slopes lower than unity. These linear correlations re-state that the electron exchange and Coulombic integral also vary proportionally to the potential differences. From these correlations, it is possible to determine Es and ET of those boron complexes that do not give fluorescence and phosphorescence.
    Zusätzliches Material: 5 Ill.
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  • 72
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 21-28 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The interaction of benzo-15-crown-5, benzo-18-crown-6, dibenzo-18-crown-6, dibenzo-24-crown-8, and dibenzo-30-crown-10 with tropylium tetrafluoroborate in 1,2-dichloroethane was studied by spectroscopic methods. The stoichiometries of the complexes in the gas phase were investigated by fast atom bombardment mass spectrometry. The crown ethers formed 1:1 molecular complexes with the acceptors, apparently by a charge-transfer mechanism. The stability constant K and the molar absorptivity of the complex εc were determined by the method of Rose and Drago. The magnitudes of the thermodynamic parameters of complexation were calculated. A discussion of the thermodynamic parameters is included.
    Zusätzliches Material: 4 Ill.
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  • 73
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 29-34 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The relative reactivity of heteroatomic compounds (PhM; M = SeR, SnR3, TeR, I) towards BuLi was estimated by competitive experiments. The rates of exchange reactions in THF increase in the order I 〉 Te ≫ Sn ≫ Se with a ratio of 1000:300:15:1 at - 70 °C when R = Bu. Me3SnPh underwent exchange much faster than Bu3SnPh, suggesting that the exchange reaction was largely affected by steric hindrance. The evidence that Bu3SnPh and BuTePh react with BuLi at almost the same rate in the presence of HMPA and that the relative exchange rates of Li-Te/Li-Sn increase in less polar solvents such as Et2O and hexane indicates that coordination of solvents towards lithium plays an important role in exchange reactions. Relative activation parameters obtained from competitive reactions of PhTeBu and PhSnBu3 with BuLi showed that Li-Te exchange was favored over Li-Sn exchange by an enthalpy factor. Hammett treatment of Li-Te exchange of ArTeBu with BuLi in THF showed a substantially large positive reaction constant (ρ) of 3·4, indicating that the anion charge was largely distributed on the leaving group in the transition state.
    Zusätzliches Material: 4 Ill.
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  • 74
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 35-40 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Nitrogen and deuterium kinetic isotope effects were measured in the Menshutkin reaction between methyl iodide and a series of para-substituted N,N-dimethylanilines in ethanol. The nitrogen kinetic isotope effect increases for the more electron-donating substituents [0·9989, 1·0032, and 1·0036 for 4-C(O)Me, H and 4-Me, respectively], in agreement with the Hammond postulate. The secondary deuterium isotope effect, however, exhibits the reverse trend (1·045, 0·989, 0·975 per deuterium, for the respective substituents). This discrepancy is rationalized in terms of solvent molecule participation in the transition state.
    Zusätzliches Material: 2 Ill.
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  • 75
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996) 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 76
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 41-49 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Nitrogen, carbon and secondary deuterium kinetic isotope effects were calculated for the Menshutkin reaction between methyl iodide and para-substituted aromatic N,N-dimethylamines using quantum mechanical methods. Different semiempirical Hamiltonians and continuum solvent models were evaluated on the basis of comparison between the experimental and theoretical values of these isotope effects.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 77
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A new host compound in optically resolved and racemic forms for selective crystalline inclusion formation derived from natural mandelic acid was synthesized. Inclusion properties of the two optical species are discussed, involving comparison with a lactic acid-based host analogue. Inclusion compounds with amines, ketones and heterocyclics and specifically with small unbranched alcohols were isolated. The crystal and molecular structures of the optically resolved and racemic forms of the free host at room temperature and the methanol inclusion complex of the resolved host at 255 K were determined by x-ray analysis. Two different binding schemes characterize the packing of these structures, in which one hydroxyl group is responsible for the formation of dimers and chains while in the free host the other hydroxyl group is involved in OH···phenyl interactions. A survey of the OH ···phenyl interactions based on the Cambridge Structural Data Base (October 1994 version) reveals that π-electron bonding occurs in a wide range of crystal structures. The approximation of the hydrogen appears to take place in an asymmetric way. Several calculations for the ab initio prediction of the crystal structures were performed.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 78
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The design, synthesis and antimycotic activities of 18 (N-heteroaryl)arylmethanamines are reported. The MIC against Candida strains of the most active amine, 3-(p-methylbenzylamino)quinoline, is comparable to that of pyrrolnitrin.
    Zusätzliches Material: 3 Tab.
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  • 79
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 66-78 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Ab initio calculations at both the Hartree-Fock and Møller-Plesset (MP2) levels of theory utilizing various basis sets were carried out on propargyl alcohol and its derivatives. The results of these calculations were used in conjunction with available experimental data in the formulation of an MM3 force field for these compounds. The energetic data obtained via the ab initio calculations were modeled well within the MM3 formalism, and are in agreement with the experimental results to within 1 kcal mol-1. For those structural parameters which were the focus of this study, the calculated results agreed well with existing experimental and ab initio data. The vibrational frequencies are also in good agreement with only small deviations in a few modes of methyl propargyl ether and propargyl fluoride.
    Zusätzliches Material: 5 Ill.
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  • 80
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The gas-phase basicities of 3,4,5-tri-tert-butylpyrazole (I) and 1,3,4,5-tetra-tert-butyl-pyrazole (II) were measured by Fourier transform ion cyclotron resonance spectrometry. The x-ray molecular structures of I·HCl (a monohydrate) and II were determined. A clear lack of planarity is present in the pyrazole rings because of the steric effects of the tert-butyl substituents. The Csp3 atom bonded to N-1, C-3, C-4 and C-5 atoms deviates significantly from the pyrazole plane, as expected on the basis of semi-empirical AM1 calculations. In I·HCl, the molecules form dimers through symmetry centres in which the chlorine atom and the water molecules play an important role.
    Zusätzliches Material: 3 Ill.
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  • 81
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: This paper reports a theoretical approach based on ab initio calculations for the evaluation of intrinsic reaction constants of resonance, field/inductive and polarizability effects of compounds subject to protonation. Field/inductive and polarizability constants can be evaluated from direct relationships between δΔEp and intrinsic contributions of the substituent. On the other hand, resonance constants should be estimated from relationships between the proton charge in the protonated molecular form and the intrinsic contributions of the substituent. It is also shown that during a protonation process the change in π charge of the carbon atom that is to bear the substituent should be the most suitable index for determining the π-electron demand of the structure concerned.
    Zusätzliches Material: 4 Ill.
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  • 82
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 105-110 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The oxidation of several monosubstituted phenoxyacetic acids by pyridinium hydrobromide perbromide (PHPB) was studied in aqueous acetic acid. The reaction is first order with respect to PHPB. Michaelis-Menten-type kinetics are observed with respect to phenoxyacetic acids. The oxidation of [2,2-2H2]phenoxyacetic acid exhibits a substantial kinetic isotopic effect. The effect of solvent composition indicates that the transition state is more polar than the reactants. The formation constants of the intermediate phenoxyacetic acid-PHPB complexes and the rates of their decomposition were determined at different temperatures. The rates of oxidation of para- and meta-substituted phenoxyacetic acids were correlated with Hammett's substituent constants. The ρ value is -2·59 at 35°C. The rates of oxidation of ortho-substituted compounds are correlated with Charton's triparametric equation. A mechanism involving transfer of a hydride ion from the substrate to the oxidant is proposed.
    Zusätzliches Material: 1 Ill.
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  • 83
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A series of 23 bridgehead-substituted bicyclo[1.1.1]pentanes were synthesized and the 3J(C1-H) coupling constants determined from their proton-coupled 13C NMR spectra. It was found that the values of the couplings are strongly dependent upon the type of substituent present, with powerful effects exerted by the halogens in particular. The IPPP-CLOPPA-INDO theoretical approach, which was employed to provide a measure of the extent of through-bond versus through-space transmission of coupling information, was found to give 3J(C1-H) values in good agreement with experimental data. Empirical substituent parameter regressions were performed and found to be consistent with the CLOPPA description of the increase in both the through-bond and through-space contributions to the coupling. The substituent parameter regressional analyses also demonstrated that electronegativity effects play a predominant role in determining the magnitude of the couplings, particularly in those substrates in which the substituent is attached to the ring system by a second-row element.
    Zusätzliches Material: 4 Ill.
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  • 84
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The molecular and crystal structures of two crystalline forms of hexa(pyrazol-1-yl)benzene were determined by x-ray analysis. They correspond to two conformational polymorphs: form I is obtained in acetic acid and form II in ethanol or dichloromethane. The crystal packing of both conformers is different; however, that of form I is analogous to that of hexa(3,5-dimethylpyrazol-1-yl)benzene, having similar cell dimensions and space groups R-3. No significant interactions except the van der Waals interactions were observed. Semiempirical calculations at the AM1 and SAM1 levels, exploring all possible conformations of the pyrazole rings, reveal that the most stable conformation presents the pyrazole rings with the N(2) alternating between both sides of the phenyl plane as it occurs in the solid state, crystalline form I (conformation 8h). The computed minimum energy for conformer 7a, which is related to crystal form II, presents a different sequence of pyrazole arrangements [N(2) up or down] and is only 1·6-2·0 kcal mol-1 less stable than the previous one in both parametrizations. The SAM1 method yields pyrazole moieties more perpendicular to the benzene ring than the AM1 one.
    Zusätzliches Material: 8 Ill.
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  • 85
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996) 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 86
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996) 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 87
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Pseudo first-order rate constants (kobs1) for methanolysis of ionized phenyl salicylate (PS-) show a decrease of 3-5-fold with increase in CH3CN content from 2 to 60 or 70% (v/v) in mixed aqueous solvents containing 0·01 mol dm-3 LiOH and a constant content of CH3OH. At 0·01 mol dm-3 KOH, the rate constants, kobs1, reveal a decrease of 15-20% and an increase of 70-130% with increase in the CH3CN content from 2 to 30% (v/v) and from 30 to 60 or 70% (v/v) respectively. The values of ΔH
    Zusätzliches Material: 1 Ill.
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  • 88
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 287-294 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Stereoselectivities and rates of Diels-Alder reactions in different solvents were correlated with a parameter, Q, defined based on internal pressure, which is normalized with respect to a polarity scale. The polarity scale or index, although purely empirical in nature, can be calculated from the refractive index of the solvent. These correlations were linear for both stereoselectivities and reaction rates. Using expressions derived in this study, it is possible to represent the kinetic profiles of several Diels-Alder reactions in about 75 pure and mixed solvent media. The activation volume of a reaction can be directly estimated from the regression of data on rates and Q in various solvents using the proposed correlations.
    Zusätzliches Material: 4 Ill.
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  • 89
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 348-354 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The molecular gas-phase elimination kinetics of the series (Cl(CH2)nCOOH (n = 1-4), show changes in mechanisms from polar five-centered intramolecular displacement of the Cl leaving group by the acidic hydrogen of the COOH to neighboring group participation of the oxygen carbonyl of the COOH group. The mechanisms for the series 2-, 3- and 4-chlorobutyric acids are explained similarly as above. The leaving chloride at the 2-position of acetic, propionic, and butyric acids is displaced by the hydrogen of the COOH group through a prevaling path of a five- centered cyclic transition-state mechanism. This type of mechanism is also described for the pyrolysis of 2-hydroxy-, 2-alkoxy-, 2-phenoxy-, and 2-acetoxycarboxylic acids. The ease with which the groups at the 2-position of acetic and propionic acids are displaced by the H of COOH give rise the sequences AcO 〉 OH 〉 PhO 〉 EtO 〉 MeO 〉 Cl and AcO 〉 PhO 〉 Br 〉 EtO 〉 MeO 〉 MeO 〉 OH 〉 Cl, respectively. These two sequences differ only in the OH leaving group position. Additional work on glycolic acid pyrolysis is needed to explain the above differences.
    Zusätzliches Material: 8 Tab.
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  • 90
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 398-402 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The kinetics of complex formation between Pd(H2O)42+ and S-carboxymethyl-L-cysteine (SCMCH2) was investigated in the presence of sodium dodecyl sulphate in the acidity range between 2 M HClO4 and pH 5. Although the mechanism was not affected by the presence of anionic micelles, retardation (2·2 〈 pH 〈 5) and acceleration (pH 〈 2·2) of the complex formation were observed compared with its rate in aqueous solution. These effects were interpreted in terms of the long-range electrostatic interactions between the negatively charged micellar surface and ligand species which can be in different ionic forms depending on the pH.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 91
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 381-386 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Electrical currents trigger oxidation or reduction reactions in conducting polymers. Changes in volume associated with these redox processes can be transformed into macroscopic movements of more than 180° by the construction of a bilayer: polypyrrole-flexible and inactive polymer (artificial muscle). The effects of the applied potential, the nature of the solvent and the electrolyte concentration on the angular movement of the free end of the bilayer were analysed. The movement accelerates with increasing anodic (or cathodic, when the movement is reversed) overpotentials, with increasing electrolyte concentration or by using more polar solvents, leading to the conclusion that the movement is linked to electrochemically driven exchange of hydrated counterions between the solution and the conducting polymer. Geometrical considerations give a simple equation for both the microscopic and macroscopic changes of volume associated to the penetration of counterions during oxidation, which is able to explain the experimental behaviour.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 92
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 427-432 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Molecular volumes of 80 compounds (50 liquids and 30 solids), with densities in the range 0·6-3·0 g cm-3, were calculated by molecular mechanics. The densities derived from these molecular volumes (Vmol MM) by the approximation dMM = mol. wt/Vmol MMNA (NA = Avogadro's number) give two linear correlations (one for liquids and one for solids) when plotted versus experimental densities. Two general equations obtained from those relationships give a good precision (3% mean error) when tested in the calculation of the experimental densities of 183 compounds that have different structures and functional groups.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 93
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The effect of temperature on the Dimroth-Reichardt ET(30) parameter of binary mixtures of dimethyl sulfoxide, acetonitrile and nitromethane with alcohols and water was studied. The ET(30) polarity parameter of many of these binary mixtures exhibits a strong synergism. Dimethyl sulfoxide, acetonitrile and nitromethane form hydrogen-bonded complexes with the alcohols more polar than themselves. The ET(30) values of the mixtures were fitted according to an earlier model, based on solvent exchange equilibria, that allows calculation of the ET(30) values of the hydrogen-bonded complexes. The variation of the ET(30) values of the pure solvents and the hydrogen-bonded complexed solvents with temperature shows that the synergism decreases as the temperature increases.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 94
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 436-438 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Carbon-bridged [1.1]ferrocenophanes have generally been assumed to have syn structures, since anti isomers have been considered to be too strained. The recent discovery that such compounds may crystallize as anti isomers raises the question of whether the compounds prefer anti or syn conformations in solution. The synthesis of β-acetyl-[1.1]ferrocenophane (1) and its investigation by 1H,1H-NOESY are reported. Compound 1 was found to be a rapidly equilibrating mixture of syn isomers in CDCl3 at 22 °C.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 95
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 411-418 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The autoxidation of various retinyl polyenes and carotenoids in chlorobenzene at 45°C and in thin solid films on a support at room temperature was investigated. The compounds used were β-carotene, canthaxanthin, retinyl acetate, methyl (all-E)-retinoate, methyl (13Z)-retinoate, retinal, C18 ketone, β-ionylidene acetaldehyde, ψ-ionone, β-ionone and ethyl sorbate as a model compound. It was shown that the isomerization of polyenyl peroxy radicals occurs during autoxidation of all the compounds studied, excepting β-ionone. A kinetic scheme for the polyene autoxidation process was considered and analysed. The conditions under which the rate constants of elementary reactions may be determined were defined and the rate constants of propagation and termination reactions for different polyenes were evaluated. The disappearance and formation of different functional groups were monitored by the spectroscopic investigation of autoxidation of polyene solid films. Mechanisms of the initial stages of the process are proposed for different polyenes.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
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  • 96
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Structures of 14 kinds of benzylic cations into which are introduced various substituents at benzylic position were optimized by means of the ab initio molecular orbital method at the RHF/6-31G* level. The theoretical indices obtained associated with the resonance interaction, such as population, bond order and bond length, were compared with the resonance demand parameter (r value) of corresponding solvolysis systems that were given by the Yukawa-Tsuno substituent effect analysis. The r value was linearly correlated with the theoretical resonance indices.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
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  • 97
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 529-538 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Substituent effects in the aminium salt catalyzed Diels-Alder reactions of 2,3-dimethyl-1,3-butadiene with a series of meta and para substituted β-methylstyrenes are used to probe detailed mechanistic aspects of these reactions. Kinetic studies were carried out using two different aminium salt catalysts and also electrochemically, using anodic potentials corresponding to the oxidation potentials of the aminium salts. Substituent effects in the equilibrium oxidations of the styrene substrates to the corresponding cation radicals were also studied, via oxidation potential measurements. The results indicate rate determining one electron oxidation of the sytrenes to their cation radicals via an outer sphere electron transfer.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 98
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 545-551 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The reaction of barbiturate and 1,3-dimethylbarbiturate ions with o-, p- and 2,4-dinitrobenzaldehyde was studied. The reactions of barbiturate anion with o- and p-nitrobenzaldehyde exhibit a pH-rate profile different to that the corresponding to the reactions of barbiturate and 1,3-dimethylbarbiturate ions with 2,4-dinitrobenzaldehyde. The dependence of the rate constant on the viscosity of the medium in the pH range 2-4, for all the reactions, indicates the contribution of a diffusion-controlled proton transfer from the hydronium ion to an addition intermediate, T-, in the rate-determining step. Surprisingly, in the reaction of 2,4-dinitrobenzaldehyde with barbiturate and 1,3-dimethylbarbiturate anions, the Brønsted plot for general acid catalysis for carboxylic acids of pKa between 2 to 5 gives a linear relationship with α = 0·707 (r = 0·991), whereas α = 0 is expected, considering the pKa of the addition intermediate T-. On the other hand, the point for the rate constant, considering water as a general acid catalyst, falls approximately 105 times above the corresponding Brønsted line. The tautomerism existing in the intermediate T- permits these surprising facts to be explained.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 99
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 583-587 
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 3-Chloro-2,2-dimethylpropan-1-ol was pyrolysed in a static system at 410·0-459·1 °C and 62-179 Torr. The reaction, in a seasoned vessel and in the presence of the free radical suppressor propene, is homogeneous, unimolecular, and follows a first-order rate law. The rate coefficient follows the Arrhenius equation: log k1 (s-1) = (13·14±0·15) - (218·8 ± 2.1) kJ mol-1 (2·303RT)-1. The products are isobutene, formaldehyde and HCl gas. The exclusive intramolecular migration of the CH2OH group to the positively charged carbon atom, from the C(SINGLE BOND)Cl bond polarisation, appears to proceed by way of an intimate ion-pair type of mechanism. The intermediate 3-methylbut-3-en-1-ol, under the reaction conditions, undergoes a six-centered decomposition characteristic of β-hydroxyalkenes to produce isobutene, formaldehyde and HCl. The pyrolysis of the deuterated substrate, 3-chloro-2,2-dimethylpropan-1-[2H]ol, serves to support the mechanistic consideration assumed above.
    Zusätzliches Material: 7 Tab.
    Materialart: Digitale Medien
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  • 100
    ISSN: 0894-3230
    Schlagwort(e): Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Geometries of secondary and tertiary benzylic cations, which have bulky substituents at α positions, were optimized by ab initio MO calculations at the RHF/6-31G* and, in part, MP2/6-31G* levels. Calculated øcalc, which is the dihedral angle of the α-C (SINGLE BOND) C bond with respect to the aromatic plane, is compared with the relative resonance demand r/rmax obtained from solvolysis reactivity and also cation stability; r and rmax are the resonance demand in the Yukawa(SINGLE BOND)Tsuno equation for any given system examined and the corresponding ideal full-resonance stabilized demand, respectively. The results suggest that there is a close relationship between the experimental and calculated relative resonance demands expressed by r/rmax = cos2 øcalc, which is suggested by HMO theory for the resonance interaction in the benzyl cation. Thus the r value is a good parameter indicating the degree of resonance interaction between benzylic 2p π-orbital and the benzene π-system.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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