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  • 1990-1994  (606)
  • 1980-1984
  • 1993  (606)
  • Computational Chemistry and Molecular Modeling  (478)
  • Nuclear reactions
  • pharmacokinetics
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  • 1990-1994  (606)
  • 1980-1984
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  • 101
    ISSN: 1573-904X
    Keywords: succinylated human serum albumin ; anti-HIV compound ; pharmacokinetics ; perfused rat liver
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract After intravenous injection of a low dose (25 µg/kg) in rats, the anti HIV-1 compound succinylated human serum albumin (Suc-HSA) is taken up mainly in the liver and spleen and is proteolytically degraded. Ten minutes after injection of 125I-Suc-HSA, 72 and 14% of the dose were found in the liver and spleen, respectively. With immunohistochemistry we demonstrated that in both organs, Suc-HSA was specifically endocytosed in endothelial cells. In the isolated perfused rat liver preparation, liver uptake was shown to be saturable, with a K m of 2.9 10−8 M and a V max of 2.4 µg/inin/100 g body weight. The apparent K m and V max in vivo were 2.2 10−7 M and 10.3 µg/min/100 g, respectively. Uptake in liver and spleen was inhibited by preadministration of an excess of formaldehyde-treated albumin and with polyinosinic acid, indicating the involvement of the scavenger receptor, as anticipated for such polyanionic compounds. Suc-HSA is not absorbed intact from the colon and the ileum. After injecting (i.v.) rats with a high dose of Suc-HSA (10 mg/kg), the elimination t 1/2 was 3 hr, and therefore, sustained plasma levels above the concentration needed for in vitro anti-HIV-1 activity can be achieved.
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  • 102
    ISSN: 1573-904X
    Keywords: bidisomide ; absorption sites ; pharmacokinetics ; man
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Absorption and disposition of bidisomide were studied in 12 healthy male subjects after a 20-min iv (1 mg/kg; N = 6) infusion and oral (2 mg/kg; N = 6) administration of the 14C-labeled drug. The oral absorption profile of unlabeled bidisomide was also studied after administration of a solution by a nasoenteric tube to different sites of the gastrointestinal tract (stomach, duodenum, jejunum, and ileum). The systemic availability was 61%. Absorption was slow initially and then rapid, achieving peak plasma concentrations between 2 and 4 hr. Less than complete systemic availability was attributed to incomplete absorption rather than first-pass metabolism. When the drug solution was delivered directly to the stomach, two distinct peak plasma levels were found. This was attributed to the more rapid absorption of bidisomide in the duodenum and ileum (and/or possibly colon). Following an iv dose, plasma levels of the drug declined with mean half-lives of 0.11, 2.0, and 12 hr for α, β, and γ phases, respectively, and a plasma clearance of 380 mL/min. The percentages of the dose recovered as bidisomide in urine and feces were 19 ± 1 and 29 ± 4 for the iv dose and 9.1 ± 0.9 and 48 ± 5 for the oral dose. Bidisomide did not exhibit substantial enantioselective pharmacokinetics in plasma regardless of the route of administration. The mean urinary excretion of the (–) enantiomer was, however, slightly higher than that of the (+) enantiomer, with (–)/(+) enantiomeric ratios of 1.2 and 1.3 after iv and oral administration, respectively. The enantiomeric ratio of bidisomide recovered in the feces was approximately 1.
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  • 103
    Electronic Resource
    Electronic Resource
    Springer
    Pharmaceutical research 10 (1993), S. 165-170 
    ISSN: 1573-904X
    Keywords: neural network ; neurocomputing backpropagation ; modeling ; pattern recognition ; pharmacodynamics ; pharmacokinetics ; classification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Neurocomputing is computer modeling based, in part, upon simulation of the structure and function of the brain. Neural networks excel in pattern recognition, that is, the ability to recognize a set of previously learned data. Although their use is rapidly growing in engineering, they are new to the pharmaceutical community. This article introduces neurocomputing using the backpropagation network (BPN).
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  • 104
    ISSN: 1573-904X
    Keywords: neural computing ; prediction ; pharmacokinetics ; humans ; animals ; allometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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  • 105
    Electronic Resource
    Electronic Resource
    Springer
    Pharmaceutical research 10 (1993), S. 598-602 
    ISSN: 1573-904X
    Keywords: capillary ultrafiltration ; in vivo sampling ; pharmacokinetics ; acetaminophen ; theophylline ; subcutaneous tissue
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Capillary ultrafiltration probes were utilized for in vivo sampling of therapeutic drugs in awake rats. Capillary ultrafiltration probes implanted into subcutaneous tissue were able to follow the disposition of acetaminophen and theophylline. Ultrafiltration probes provided samples at a rate of 2–3 µL/min. Ultrafiltrates were analyzed by liquid chromatography with either UV or electrochemical detection. Simultaneous ultrafiltration and microdialysis probes and multiple ultrafiltration probes were used in individual animals to validate the technique. The pharmacokinetics of two well-established drugs, acetaminophen and theophylline, were monitored in awake, freely moving rats to demonstrate the viability of the technique. The half-life for acetaminophen was determined to be 20.9 ± 1.0 min (n = 6) for a 2 mg/kg dosing. The half-life of elimination for theophylline was determined to be 3.0 ± 0.1 hr (n = 4) for a 4 mg/kg dose. The capillary ultrafiltration probes exhibited a constant flow rate of 2.4 ± 0.1 µL/min and removed 50 nL/min/mm of fluid from the extracellular space. Capillary ultrafiltration sampling is shown to be an excellent tool for in vivo monitoring of drug disposition and a suitable method for determining pharmacokinetic parameters in awake animals.
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  • 106
    ISSN: 1573-904X
    Keywords: procaterol ; bronchodilator ; healthy volunteers ; pharmacokinetics ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics and relative oral bioavailability of procaterol, an orally active β2-adrenergic agonist bronchodilator were evaluated in healthy volunteers. Procaterol was rapidly absorbed after oral administration. Mean plasma procaterol concentration–time profiles and pharmacokinetic parameters for both formulations were essentially superimposable. Following tablet administration, the mean C max was 358 pg/mL and the corresponding mean t max was 1.6 hr. Mean renal clearance was 163 mL/min and accounted for approximately one-sixth of the mean apparent oral plasma clearance (988 mL/min). The mean apparent elimination half-life of procaterol was 4.2 hr. Hepatic metabolism appears to be the primary mechanism for elimination of procaterol from the body, and first-pass metabolism may limit systemic bioavailability.
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  • 107
    ISSN: 1573-904X
    Keywords: Fab fragment ; radioimmunoassay ; pharmacokinetics ; urinary metabolites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Anti-sheep Fab fragment antisera were produced in rabbits using sheep digoxin-specific Fab fragments (Digidot) as immunogen. These antisera were used for the development of a radioimmunoassay (RIA) of sheep Fab fragments in human plasma and urine using 125I-labeled Fab fragments. Interference in the assays by digoxin, human proteins, and antibodies from different species was insignificant, but cross-reactivity between anti-sheep Fab antisera and goat IgG or Fab fragments was 22 to 67%. The limit of detection was 0.1 µg/mL and the assay was linear over a 0.6–28 µg/mL range of Fab fragments. Intra- and interassay coefficients of variation were less than 6.9 and 10.5%, respectively. Accuracy of plasma and urine assays at various Fab fragment levels ranged from 96 to 106%. RIA was applied to the pharmacokinetic study of sheep digoxin-specific Fab fragments in one patient acutely intoxicated by digitoxin and treated with Digidot. The Fab elimination half-life was 12.1 hr. Steady-state volume of distribution and total-body clearance were 10.8 L and 23.4 mL/min, respectively. Unchanged Fab fragments (50 kD) and degradation products (25 kD) isolated by gel filtration chromatography of a urine sample cross-reacted with the anti-Fab antiserum.
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  • 108
    ISSN: 1573-904X
    Keywords: drug targeting ; sugar recognition ; glycosylated dextran ; pharmacokinetics ; cytosine β-D-arabinoside
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract To develop a new carrier system for hepatic targeting, carboxymethyl-dextran (CMD) was modified with galactose and mannose residues (Gal-CMD, Man-CMD), and their disposition characteristics were studied in mice using 14C-labeled dextran. At a dose of 1 mg/kg, i.v.-injected Gal-CMD and Man-CMD rapidly accumulated in the liver parenchymal and nonparenchymal cells, respectively, because of their preferential uptake via carbohydrate receptors in these cells. Pharmacokinetic analysis revealed that their uptake rates were sufficiently large for selective drug targeting. Targeting of cytosine β-D-arabinoside (araC) was studied using Gal-CMD as a specific carrier to the hepatocytes. From the conjugate of araC with Gal-CMD, araC was released with a half-life of 36 hr in phosphate buffer (pH 7.4) and 23 hr in plasma. An in vivo biodistribution study demonstrated a disposition profile of the conjugated araC similar to that of the carrier, and selective delivery to hepatocytes of up to 80% of the dose was achieved. These findings suggest that glycosylated CMDs are carriers with a high affinity to liver parenchymal or nonparenchymal cells without any affinity to other tissues.
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  • 109
    ISSN: 1573-904X
    Keywords: pharmacokinetics ; double peaks ; dose-dependent absorption ; intestinal excretion ; exsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The elimination of [3H]pafenolol and metabolites was investigated in fasted and fed rats. Separate groups received intravenous doses (0.3 and 3.0 µmol/kg) and oral doses (1 and 25 µmol/kg). After iv administration of pafenolol, the excretion of unchanged drug into urine and feces was about 50 and 25–30% of the given dose, respectively. The predominating mechanism for the excretion of pafenolol into feces was intestinal excretion (exsorption) directly from blood into gut lumen, since only about 3% of a given iv dose was recovered as pafenolol in the bile. When the oral dose was raised from 1 to 25 µmol/kg, the mean (±SD) bioavailability, calculated from urine data, increased from 14 ± 9 to 30 ± 11% (P 〈 0.05) in the starved rats and from 14 ± 3 to 16 ± 3% in the fed animals. In parallel, the fraction absorbed from the gut (f a) increased from 19 ± 9 to 31 ± 10% in the starved rats and from 16 ± 4 to 19 ± 5% in the fed animals, respectively. This indicates that the low bioavailability is due primarily to poor intestinal uptake.
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  • 110
    ISSN: 1573-904X
    Keywords: diltiazem ; sustained-release preparation ; pharmacokinetics ; metabolism ; colon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Pharmacokinetics of diltiazem and its six metabolites were compared after oral administration in dogs of a multiparticulate sustained-release diltiazem preparation (HER-SR, QD) and a conventional diltiazem preparation (HER, TID). The plasma concentration of diltiazem, its two active basic metabolites (Ml, N-monodesmethyl diltiazem; M2, deacetyl diltiazem), and four acidic metabolites [Al, ( + )-(2S,3S)-2-(4-methoxyphenyl)-3-acetoxy-4-oxo-2,3,4,5,-tetrahydro-l,5-benzothiazepin-5-acetic acid; A2, 3-deacetyl-Al; A3, O-demethyl-Al; A4, O-demethyl-3-deacetyl-Al] following several administration routes were determined using high-performance liquid chromatography with UV detector (UV-HPLC). Following the oral administration of HER to dogs, plasma concentrations were in the descending order of A2, diltiazem, Ml, and M2. The absolute bioavailability of diltiazem was about 30%. Diltiazem conversion to its metabolites (Ml, M2, A2) was 31.0, 2.1, and 14.6%, respectively. Following intraduodenal and mesenteric venous administration of diltiazem, Ml and A2 were produced mainly in the intestine and liver. Oral administration of HER-SR and HER to dogs resulted in almost-identical plasma concentrations of A2, diltiazem, Ml, and M2 (descending order). Supported evidence was the effective absorption of diltiazem from all gastrointestinal tract regions and similar formation ratios of diltiazem basic metabolites (Ml, M2) from the duodenum, ileum, and colon.
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  • 111
    Electronic Resource
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    Springer
    Journal of pharmacokinetics and pharmacodynamics 21 (1993), S. 323-334 
    ISSN: 1573-8744
    Keywords: toxicology ; pharmacokinetics ; AUC ; CxT
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Five major objectives for pharmacokinetic investigations in support of toxicity studies are identified as follows: Assess whether animals exhibited measurable blood concentrations in a dose-dependent manner; estimate average area under the concentration- time curve (AUC)and maximal concentration (C max )for each treatment group; elucidate general patterns in the concentration-time (CxT)profile, and summarize relationships between CxTand treatment group; determine CxTdependence on day into study; and judge interanimal variability and identify any animals with unusual concentration response. Such objectives are generally addressed in rodent toxicity studies by including “satellite” animals in the study. Satellite animals are extra animals dosed as per protocol but not subjected to toxicological and pathological observations and tests. Instead, they are used exclusively for the evaluation of pharmacokinetic characteristics of the test compound. In this paper, methods are described for achieving the five listed pharmacokinetic objectives in rodent toxicity studies without the use of satellite animals. A rat toxicity study is presented as an example.
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  • 112
    Electronic Resource
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    Springer
    Journal of pharmacokinetics and pharmacodynamics 21 (1993), S. 639-651 
    ISSN: 1573-8744
    Keywords: plasma protein binding ; Michaelis-Menten elimination ; pharmacokinetics ; flavone acetic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Flavone acetic acid (FAA) is an antineoplastic agent that has undergone extensive study in Phase I trials. Concentration-dependent plasma protein binding has been demonstrated in vitroconcentrations of total drug that are achieved in vivo.Moreover, dose-dependent total systemic clearance has been described when FAA has been administered as a short iv infusion. When administered as a prolonged 24-hr infusion, total FAA (bound plus unbound) plasma pharmacokinetics are well described with a first-order two-compartment model. However, measurement of unbound FAA intra- and post-intravenous infusion in eight patients revealed a twofold increase in fraction of FAA unbound in plasma intrainfusion. We attempted to fit pharmacokinetic structural models of varying complexity to the unbound concentrations alone and simultaneously to the unbound and bound FAA plasma concentrations. The data were adequately described only by a model that incorporated simultaneous saturable plasma protein binding and a Michaelis-Menten process for elimination. A comparison among models is presented, as well as pharmacokinetic parameter estimates for FAA in children. These clinical data are consistent with predictions of the clearance model in which both saturable protein binding (resulting in a dynamically increasing unbound fraction) and saturable elimination (resulting in gradually decreasing unbound intrinsic clearance) are operative.
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  • 113
    Electronic Resource
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    Springer
    Journal of pharmacokinetics and pharmacodynamics 21 (1993), S. 735-750 
    ISSN: 1573-8744
    Keywords: interoccasion variability ; interindividual variability ; intraindividual variability ; pharmacokinetics ; population analysis ; NONMEM
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Individual pharmacokinetic parameters may change randomly between study occasions. Analysis of simulated data with NONMEM shows that ignoring such interoccasion variability (IOV) may result in biased population parameter estimates. Particular parameters affected and the extent to which they are biased depend on study design and the magnitude of IOV and interindividual variability. Neglecting IOV also results in a high incidence of statistically significant spurious period effects. Perhaps most important, ignoring IOV can lead to a falsely optimistic impression of the potential value of therapeutic drug monitoring. A model incorporating IOV was developed and its performance in the presence and absence of IOV was evaluated. The IOV model performs well with respect to both model selection and population parameter estimation in all circumstances studied. Analysis of two real data examples using this model reveals significant IOV in all parameters for both drugs and supports the simulation findings for the case that IOV is ignored: predictable biases occur in parameter estimates and previously nonexistent period effects are found.
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  • 114
    Electronic Resource
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    Springer
    Journal of pharmacokinetics and pharmacodynamics 21 (1993), S. 1-17 
    ISSN: 1573-8744
    Keywords: furosemide ; protein-calorie malnutrition ; pharmacokinetics ; pharmacodynamics ; decreased gastric and liver first-pass metabolism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of dietary protein deficiency on pharmacokinetics and pharmacodynamics of furosemide was investigated after iv bolus (1 mg/100 g) and oral (2 mg/100 g) administration of furosemide to male Sprague-Dawley rats fed on a 23% (control) or a 5% (protein-calorie malnutrition: PCM) protein diet ad lib.for 4 weeks. After iv administration, the mean values of CL R , V ss, and the percentages of dose excreted in 8-hr urine as furosemide were increased 81, 31, and 61%, respectively, in PCM rats when compared with those in control rats, however, CL NR was 54% decreased in PCM rats. The decreased CLNR in PCM rats suggested the significantly decreased nonrenal metabolism of furosemide. The urine volume per g kidney after iv administration was not significantly different between the two groups of rats although the amount of furosemide excreted in 8-hr urine per g kidney increased significantly in PCM rats. The diuretic, natriuretic, kaluretic, and chloruretic efficiencies reduced significantly in PCM rats after iv administration. After oral administration, the extent of bioavailability increased considerably from 27.6% in control rats to 47.0% in PCM rats, probably as a result of decreased gastrointestinal and hepatic first-pass metabolism. This was supported by a tissue homogenate study; the amount of furosemide remaining per g tissue after 30-min incubation of 50 μg of furosemide with the 9000 × gsupernatant fraction of stomach (42.4 vs. 47.9 μg) and liver (41.4 vs. 45.9 μg) homogenates increased significantly in PCM rats. No significant differences in CLR and t1/2 were found between the control and the PCM rats after oral administration. The 24-hr urine volume and the amount of sodium excreted in 24-hr urine per g kidney increased significantly in PCM rats, and this might be due to a significantly increased amount of furosemide reaching the kidney excreted in urine per g kidney.
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  • 115
    Electronic Resource
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    Springer
    Journal of pharmacokinetics and pharmacodynamics 21 (1993), S. 533-550 
    ISSN: 1573-8744
    Keywords: nitroglycerin ; 1,2-glyceryl dinitrate ; 1,3-glyceryl dinitrate ; pharmacokinetics ; pharmacodynamics ; clearance ; systolic blood pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Intravenous infusions of nitroglycerin (GTN), 1,2-glyceryl dinitrate (1,2-GDN), and 1,3-glyceryl dinitrate (1,3-GDN) were given to four conscious dogs at 10 μg/min, 30 μg/min, 50 μg/min, and 70 μg/min of GTN and 20 μg/min and 100 μg/min of GDNs. The steady state plasma concentrations (Css)of GTN were reached after about 60 min whereas for 1,2-GDN and 1,3-GDN the Csswere reached at about 150 min after the infusion began. Except for one dog, the Cssof GTN were not proportional to infusion rate, however, all dogs together showed a good linear relationship between Cssof GTN and infusion rates with an average correlation coefficient of 0.917±0.102. Large variability in GTN clearance after various infusion rates was observed in all dogs. The Cssratios of 1,2-GDN/GTN and 1,3-GDN/GTN yield overall averages of 31.5 ±17.2 and 5.47 ±3.19,respectively. Average Cssratios of metabolites 1,2-GDN/1,3-GDN were 5.78±1.23. This ratio is different from those obtained after iv bolus and oral dosing indicating that the biotransformation of GTN to 1,2-GDN and 1,3-GDN differs for each dosing route. The clearances for 1,2-GDN and 1,3-GDN were not changed over the dose range of 20 μg/min to 100 μg/min. Terminal half-lives of 1,2-GDN and 1,3-GDN postinfusion were similar to those values obtained after a single bolus dose (45 min). It appears that all the GTN dose at steady state can be accounted for by the formation of measurable 1,2-GDN and 1,3-GDN. Large intra- and interdog variations in systolic blood pressure decrease (SPD) following infusions of GTN were observed, however, all dogs showed a clear systolic blood pressure decrease when the highest infusion rate (70 μg/min) was given. No significant systolic blood pressure drop was detected following 20 μg/min infusions of 1,2-GDN or 1,3-GDN. It was clear that systolic blood pressure in all dogs decreased following 100 μg/min infusions of 1,2-GDN or 1,3-GDN. When SPD values were plotted vs. log GTN concentrations following the infusion of 70 μg/min of GTN in all four dogs, a counterclockwise hysteresis was observed indicating the significant contribution of the active dinitrate metabolites to GTN pharmacodynamics.
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  • 116
    ISSN: 1573-2568
    Keywords: mesalazine ; pharmacokinetics ; steady state
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The bioavailability of a controlled release 5-aminosalicylic acid preparation (Pentasa) was investigated in nine healthy children after a medication period of six days (1000 mg/day) and compared with sulfasalazine (Salazopyrin) (2000 mg/day). The local bioavailability in the distal gut lumen, reflected by the 5-aminosalicylic acid concentration in the fecal water, showed comparable values after Pentasa (4.44 mmol/liter) and Salazopyrin (6.25 mmol/liter). The concentration ofN-acetyl-5-ASA was significantly higher after Pentasa, reflecting the more proximal release of 5-aminosalicylic acid compared with Salazopyrin. No relation was found between the 5-aminosalicylic acid fecal water concentration and the 5-aminosalicylic acid dose per kilogram of body weight. The urinary excretion of 5-aminosalicylic acid andN-acetyl-5-aminosalicylic acid was higher after Pentasa than after Salazopyrin (32% vs 25%). Dose interval plasma concentration curves showed low values after both preparations. Based on the concept that the fecal water concentration is decisive for the efficacy of 5-aminosalicylic acid in distal inflammatory bowel disease, Pentasa treatment offers a relevant alternative in cases of Salazopyrin intolerance or allergy in children. The higher systemic bioavailability from Pentasa warrants monitoring of the renal function.
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  • 117
    ISSN: 1573-0646
    Keywords: menogaril ; phase I ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Thirty-five patients with advanced refractory cancer were enrolled on this phase I study of menogaril administered orally every 4 weeks at dosages ranging from 85 mg/m2 to 625 mg/m2. An additional 12 patients received alternating oral and IV doses of menogaril (250 mg/m2 IV; 250–500 mg/m2 oral) with accompanying blood and urine sampling for pharmacokinetics analysis. Nausea and vomiting were the dose-limiting toxicities at the 625 mg/m2 dosage level; vomiting was inadequately relieved by prophylactic antiemetics at this dosage level. Other toxicities included sporadic leukopenia at all dosage levels; at dosages of 500 mg/m2 and 625 mg/m2, leukopenia 〈 3000/μl occurred in 7 of 24 patients. Anemia and thrombocytopenia were much less frequent toxicities. Among the patients receiving IV menogaril, peripheral vein phlebitis, leukopenia and anemia were the predominant toxicities. No antitumor responses were observed, yet one patient with nonsmall cell lung cancer experienced a 30% reduction in metastatic tumor nodules. For the patients receiving alternating oral and IV menogaril, comparative pharmacokinetic analyses were performed by HPLC. After oral administration, maximum plasma concentrations were achieved in an average of 6 hours; maximum plasma concentrations were less than one-quarter of those achieved after intravenous administration. The harmonic mean (±SD) terminal disposition half-life after oral dosing was 29.3 ±9.2 hours; mean systemic bioavailability was 33.6±10.5% after oral dosing. Forty-eight hours after an oral dose, mean cumulative urinary excretions of menogaril and the primary metabolite, N-demethylmenogaril, were 4.00±0.96% and 0.44±0.16%, respectively. Because of the poor tolerance of oral menogaril and minimal evidence of biological activity, this schedule of drug administration is not recommended for phase II evaluation. Based on this and other published studies of oral menogaril, frequent chronic low-intermediate dosages of the drug may be given orally with potentially better tolerance and antitumor activity.
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  • 118
    ISSN: 1573-0646
    Keywords: vinca alkaloids ; vinorelbine ; pharmacokinetics ; high-pressure liquid chromatography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary We have investigated the pharmacokinetics of the investigational semi-synthetic vinca alkaloid vinorelbine (navelbine, NVB). The analyses have been performed by using a sensitive and selective method based on ionexchange normal phase high-performance liquid chromatography with fluorescence detection combined with liquid-liquid extraction for sample clean-up. Pharmacokinetic studies were performed in male FVB mice receiving 12 mg/kg NVB through intravenous injection. The results have been compared to those obtained for vinblastine (VBL). The plasma pharmacokinetics of NVB can be described by a three compartment model. The elimination half-life is significantly longer and the plasma AUC values higher for NVB compared to VBL. This is reflected in tissues, where, 24 hr after drug administration, the concentration of NVB is 5 to 10-fold higher compared to VBL. Qualitatively, the tissue distribution and retention of the drugs is very similar. The drug concentrations in most tissues decline parallel with the circulating plasma levels, whereas prolonged retention is found in tissues of lymphatic and testicular origin. Deacetylation yielding deacetylnavelbine (DNVB) is the primary metabolic route for NVB. This cytotoxic metabolite accounts for a substantial part of the overall disposition of drug. Only 58% of the administered dose is excreted in the urine (17%) and faeces (41%) as NVB or DNVB. No other metabolites have been detected.
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  • 119
    ISSN: 1573-0646
    Keywords: menogaril ; anthracycline ; pharmacokinetics ; acute leukemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Fifteen patients with relapsed or refractory acute leukemia were treated in this phase I study of menogaril (7-con-O-methylnogarol), a nogalamycin anthracycline derivative. Doses ranged from 50 mg/m2/day to 130 mg/m2/day, administered daily for 5 days. Pharmacokinetic studies were performed at each dose level and confirmed the findings of pharmacokinetic data derived from previous studies in patients with solid tumors. All patients experienced grade 4 hematologic toxicity and the dose limiting toxicity was mucositis. Two patients, one with acute myeloid leukemia and one with acute lymphoid leukemia, achieved complete responses. The AML complete response lasted 10 months and the ALL patient died in CR at 2 + months. Both patients were treated at a dose of 100 mg/m2/day for five days. At this dose, a second induction or consolidation course could be given without severe mucositis, and this is the dose recommended for further phase II studies in leukemia using this schedule.
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  • 120
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    Pharmaceutical research 10 (1993), S. 8-13 
    ISSN: 1573-904X
    Keywords: oral administration ; mean residence time ; reversible metabolism ; first-pass metabolism ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Equations for the mean residence times in the body (MRT) and AUMC/AUC of a drug and its metabolite have been derived for an oral drug undergoing first-pass and linear reversible metabolism. The mean residence times of the drug or interconversion metabolite in the body after oral drug are described by equations which include the mean absorption time (MAT), the mean residence times of the drug or metabolite in the body after intravenous administration of the drug, the fractions of the dose entering the systemic circulation as the parent drug and metabolite, and the systemically available fractions of the drug (F p p) or metabolite (F m p). Similarly, the AUMC/AUC of the drug and metabolite after oral drug can be related to the MAT, ratios of the fraction of the dose entering the systemic circulation to the systemically available fraction, the first-time fractional conversion of each compound, and AUMC/AUC ratios after separate intravenous administration of each compound. The F p p and F m p values, in turn, are related to the first-pass availabilities of both drug and metabolite and the first-time fractional conversion fractions. The application of these equations to a dual reversible two-compartment model is illustrated by computer simulations.
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  • 121
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    Pharmaceutical research 10 (1993), S. 22-27 
    ISSN: 1573-904X
    Keywords: organic mononitrates ; pharmacokinetics ; urinary recoveries ; urinary conjugation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics and urinary recoveries of four isomeric mononitrates, L-isoidide mononitrate (L-IIMN), isosorbide-2-mononitrate (IS-2-MN), isomannide mononitrate (IMMN), and isosorbide-5-mononitrate (IS-5-MN), were investigated at an intravenous dose of 2 mg/kg in rats. All four compounds exhibited monoexponential kinetics at this dose. The volumes of distribution were similar for all four isomers and were estimated at about 1.0 liter/kg. The systemic clearances of L-IIMN, IMMN, IS-2-MN, and IS-5-MN were 65.1 ± 13.0, 32.7 ± 12.0, 11.0 ± 2.3, and 8.23 ± 1.82 ml/min/kg, respectively (P 〈 0.05, all pairwise comparisons). Free mononitrate in the urine accounted for 0.306 to 4.56% of the administered dose, while the recovery in conjugated forms (after glusulase hydrolysis) accounted for 42.8% of the IMMN dose and 7.70 to 14.5% of the dose of the remaining three isomers. The dose-dependent pharmacokinetics of three of the mononitrates were explored at selected higher doses which cause equivalent vasodilator responses, L-IIMN (22 mg/kg), IS-2-MN (100 mg/kg), and IS-5-MN (300 mg/kg). The clearances of L-IIMN, IS-2-MN, and IS-5-MN at these higher doses were 42.3 ± 5.7, 6.38 ± 0.59, and 3.33 ± 0.62 ml/min/kg, respectively, all significantly less than those found at the 2 mg/kg dose. Typical Michaelis–Menten-type curvatures were observed in the concentration–time curves after IS-2-MN and IS-5-MN dosing. The pharmacokinetics of L-IIMN were also dose dependent, but they could not be described by simple Michaelis–Menten kinetics.
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  • 122
    ISSN: 1573-904X
    Keywords: pharmacokinetics ; oral absorption ; intestinal permeability ; bioavailability ; double-peaks ; dose dependency
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The gastrointestinal absorption characteristics of pafenolol following oral administration as a solution in man and rat has previously been found to be a double-peak phenomenon and exhibited dose-dependent bioavailability, despite negligible presystemic metabolism. In both man and rat the first peak appeared approximately 0.5–1 hr postdose and the second, more pronounced peak 3–4 hr postdose. In rat more than 90% of the available dose was absorbed during the second peak. In the present study we investigated the absorption of a solution of pafenolol in rats after intrajejunal and intraileal administration. The resulting blood concentration–time profile of pafenolol exhibited one peak only; the extent of absorption was similar to that observed when the same dose was given orally. The small intestinal transit time of the 14C-PEG 4000 solution was found to be more than 3 hr. The transit rate was higher in the proximal part of the small intestine compared to the more distal part, where the transit of the solution was staggered. In conclusion, the results of the intestinal transit time investigation and the administrations of pafenolol at different levels of the alimentary tract indicate that pafenolol is a drug with a specific absorption site located in the ileocolonic region.
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  • 123
    ISSN: 1573-904X
    Keywords: liposome ; doxorubicin ; pharmacokinetics ; polyethylene glycol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics of doxorubicin (DOX) encapsulated in liposomes containing polyethylene glycol-derivatized distearoylphosphatidylethanolamine (PEG/DSPE) were investigated in rodents and dogs. The plasma levels of DOX obtained with PEG/DSPE-containing liposomes were consistently higher than those without PEG/DSPE or when PEG/DSPE was replaced with hydrogenated phosphatidylinositol (HPI). Despite the inclusion of PEG/DSPE in liposomes, there was a significant drop in the plasma levels of DOX when the main phospholipid component, hydrogenated phosphatidylcholine, was replaced with lipids of lower phase transition temperature (dipalmitoylphosphatidylcholine, egg phosphatidylcholine), indicating that phase transition temperature affects the pharmacokinetics of liposome-encapsulated DOX. In beagle dogs, clearance was significantly slower for DOX encapsulated in PEG/ DSPE-containing liposomes than in HPI-containing liposomes, with distribution half-lives of 29 and 13 hr, respectively. In both instances, almost 100% of the drug measured in plasma was liposome-associated. The apparent volume of distribution was only slightly above the estimated plasma volume of the dogs, indicating that drug leakage from circulating liposomes is insignificant and that the distribution of liposomal drug is limited mostly to the intravascular compartment in healthy animals.
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  • 124
    ISSN: 1573-904X
    Keywords: lag time ; pharmacokinetics ; PCNONLIN ; absorption rate constant
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Lag time in pharmacokinetics corresponds to the finite time taken for a drug to appear in systemic circulation following extravascular administration. Lag time is a reflection of the processes associated with the absorption phase such as drug dissolution and/or release from the delivery system and drug migration to the absorbing surface. Failure to specify the lag time can lead to inappropriate or erroneous estimates of pharmacokinetic parameters. This has been demonstrated in the case of a one-compartment open model by the pharmacokinetic analysis of bioequivalence data from a study involving the administration of propoxyphene napsylate to human volunteers. Subsequently, pharmacokinetic and statistical analyses of data obtained from a series of 49 simulations involving a wide range of absorption and elimination rate constants (0.05 to 5.00 and 0.01 to 0.95 hr−1, respectively) showed that lag time has a substantial effect on several primary and secondary pharmacokinetic parameters.
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  • 125
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    Pharmaceutical research 10 (1993), S. 1083-1086 
    ISSN: 1573-904X
    Keywords: kappa agonist analgesic ; nasal absorption ; bioavailability ; pharmacokinetics ; ED50.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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  • 126
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    Chirality 5 (1993), S. 422-427 
    ISSN: 0899-0042
    Keywords: 2-arylpropionates ; enantiomers ; stereoselectivity ; chiral inversion ; pharmacokinetics ; bile-duct cannulated rats ; biliary excretion ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To examine the stereoselectivity of biliary excretion, the optically pure enantiomers of ketoprofen (KT), ibuprofen (IBU), and flurbiprofen (FLU) were intravenously administered to normal and bile duct-cannulated rats at 10 mg/kg. The recovery of total KT in bile was significantly higher after administration of (S)-KT than after (R)-KT [90.1 ± 3.5% vs 68.8 ± 8.2%, n =3, P 〈 0.05]. In normal rats the terminal half-life of (R)-KT was significantly shorter than that of (S)-KT after administration of (R)-KT (2.2 ± 0.6 h vs 14.3 ± 4.9 h, n = 3, P 〈 0.05). The terminal half-life of both enantiomers was significantly shorter in rats with continuous bile drainage as compared to normal rats. No significant differences in pharmacokinetic parameters could be found between both enantiomers in bile duct-cannulated animals. The total amount of IBU in bile was slightly higher after administration of (S)-IBU than after (R)-IBU administration. The percentage of (R)-IBU after (R)-IBU administration, however, was very low [(R)-IBU: 1.5 ± 0.9%, (S)-IBU: 23.4 ± 5.8%]. In normal rats the clearance of (R)-IBU was significantly higher as compared to (S)-IBU. Differences in pharmacokinetic parameters between normal and bile duct-cannulated rats were not statistically significant due to high interindividual variability. The total recovery of FLU, which was excreted in bile to a lower extent than either KT or IBU, also tended to be greater after S-enantiomer administration. Only small amounts of (S)-FLU could be recovered in bile after (R)-FLU administration. The pharmacokinetic parameters did not differ significantly between (R)- and (S)-FLU or between normal and bile duct-cannulated rats due to its low inversion rate and low excretion via bile. © 1993 Wiley-Liss, Inc.
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    Bulletin of experimental biology and medicine 116 (1993), S. 835-837 
    ISSN: 1573-8221
    Keywords: hypoxia ; pharmacokinetics ; antipyrine ; isoniazid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
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  • 128
    ISSN: 1573-8280
    Keywords: recombinant interleukin-2 ; monoclonal antibody ; immune complex ; drug delivery system ; pharmacokinetics ; natural killer cell ; anti-tumor effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We have investigated biological properties of an immune complex of recombinant interleukin-2 (rIL-2) and a monoclonal antibody against rIL-2 in mice for induction of killer cells and for anti-tumor activity. We have also examined the clearance of subcutaneously-injected immune complex in mice and compared it with that of rIL-2 alone. Plasma rIL-2 levels were sustained longer in mice given the immune complex than in mice given rIL-2 alone at a dose of 10μg/mouse, and they were detectable even at 24 hours after the administration of the immune complex, while they fell to undetectable levels by 6 hours after the administration of rIL-2 alone. A more significant portion of rIL-2 was detected in lymph nodes after subcutaneous injection of the immune complex than that of rIL-2 alone. Splenic lymphocytes from mice given the immune complex demonstrated a higher killer cell activity against YAC-1 cells than those from mice given rIL-2 alone. The immune complex also exerted more significant anti-tumor effect in a dose-dependent manner in Meth-A fibrosarcoma-bearing mice than rIL-2 alone. Our results indicate that immunocomplexing of rIL-2 with an antibody against rIL-2 provides a useful tool as the drug delivery system for cancer therapy using rIL-2.
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  • 129
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    International Journal of Quantum Chemistry 47 (1993), S. 405-423 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A numerical method is developed to obtain sequences of functions converging to the eigenfunctions of a Schrödinger operator in the Hilbert space L2(-∞, ∞), whose norm is used to introduce the criterion of convergence in the norm and we show that it guarantees the accurate computation of expected values of a symmetric operator. The method consists in solving the Dirichlet problem associated to the eigenvalue problem in the interval [-n, n] by the Ritz method, whose convergence to both eigenvalues and eigenfunctions is guaranteed by the compactness criterion. Using the asymptotic perturbation theory in L2(-∞, ∞), we prove the convergence of both eigenvalues and eigenfunctions of the Dirichlet problem to those of the unbounded system when the interval [-n, n] is expanded. The method is applied to the harmonic oscillator, the Mitra potential, as well as to the potential V(r) = r and the Coulomb and Yukawa potentials; in each case, the convergence of eigenvalues and eigenfunctions is shown. © 1993 John Wiley & Sons, Inc.
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  • 130
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    International Journal of Quantum Chemistry 47 (1993), S. 425-435 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We present a relativistic theory for the nuclear spin-spin coupling tensor within the polarization propagator approach using the particle-hole Dirac-Coulomb-Breit Hamiltonian and the full four-component wave function. We give explicit expressions for the coupling tensor in the random-phase approximation, neglecting the Breit interaction. A purely relativistic perturbative electron-nuclear Hamiltonian is used and it is shown how the single relativistic contribution to the coupling tensor reduces to Ramsey's three second-order terms (Fermi contact, spin-dipole, and paramagnetic spin-orbit) in the nonrelativistic limit. The principal propagator becomes complex and the leading property integrals mix atomic orbitals of different parity. The well-known propagator expressions for the coupling tensor in the nonrelativistic limit is obtained neglecting terms of the order c-n (n ≥ 1). © 1993 John Wiley & Sons, Inc.
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  • 131
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    International Journal of Quantum Chemistry 47 (1993), S. 437-448 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this paper, we present a symmetrical and adiabatic reaction path for hydrogen transfer from methane by methyl by an ab initio method using the 6-31G** basis set with the MP2 corrections for UHF/6-31G** optimized geometries. The theoretical barrier is fitted with the symmetric Eckart function. We, then, take thermal averages of the rate constant (k) considering the discrete nature of the C-H oscillators and the continuous character of the various low-frequency modes of the composite system. Finally, we present a linear relation between log k and temperature. It is shown that this relation gives a good description of the kinetic results of both thermal and photochemical H-transfer reactions in the region of low temperatures. © 1993 John Wiley & Sons, Inc.
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  • 132
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    International Journal of Quantum Chemistry 48 (1993) 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 133
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    International Journal of Quantum Chemistry 48 (1993), S. 151-159 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the regime of the molecular-orbital theory, a new approach beyond of the Hartree-Fock approximations is proposed. By an appropriate introduction of the quantum fluctuation into the molecular electronic ground state, the Hartree-Fock equations plus Gaussian fluctuation are obtained. Basically, the procedure proposed consists of an adequate utilization of the Gaussian approximation of the Ising model on a lattice (K.G. Wilson et al., Phys. Rep. C 12, 76 (1974)). It leads to an effective nonlinear Hamiltonian for the molecule for studying nonlinear problems in the molecular electronic structure. © 1993 John Wiley & Sons, Inc.
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  • 134
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    International Journal of Quantum Chemistry 48 (1993), S. 185-200 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We review and update a recently developed one-particle theory of N-electron systems that bears a certain resemblance to density functional (DF) theory and has been put forward by the present author. As distinct from DF theory, the new one-particle scheme applies to any N-electron eigenstate including the ground state. For the latter case, the key equations become identical to those familiar from the Kohn-Sham version of DF theory. The theory given here constitutes the basis for a consistent treatment of normal conductivity and superconductivity, which will be discussed in Part II of this article. © 1993 John Wiley & Sons, Inc.
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  • 135
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    International Journal of Quantum Chemistry 48 (1993), S. 161-183 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An explicitly connected commutator expansion for the average value of an observable in the coupled-cluster theory is derived. Specifically, it is shown that the expectation value of an operator for the state Ψ, related to the Fermi vacuum Φ by the exponential Ansatz ψ = eT Φ, is expressed as a finite commutator series containing the cluster operator T and an auxiliary operator S, defined by a linear equation involving again a finite commutator series in T. The above result is applied to derive the explicitly connected commutator form of the order-by-order many-body perturbation theory (MBPT) expansion for the expectation values and density matrices. We also show how the commutator expansion derived by us can be used as a basis for size-extensive infinite-order summation techniques. An operator technique of eliminating the nonlocal, “off-energy shell” denominators from MBPT expressions is proposed and applied to obtain compact commutator formulas for the expectation values of one- and two-electron operators through the fourth and third order, respectively, and for the correlation energy through the fifth order of perturbation theory. © 1993 John Wiley & Sons, Inc.
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  • 136
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    International Journal of Quantum Chemistry 48 (1993), S. 201-209 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We show that a consistent N-electron theory of a solid can within the Born-Oppenheimer (BO) approximation lead only to normal conductivity or to an insulating state. If one leaves the BO approximation by turning on electron-phonon interaction, one can establish a lower-lying new ground state that has the characteristic properties of the Bardeen-Cooper-Schrieffer (BSC) ground state. We demonstrate that an (N + Nn)-particle Schrödinger equation that describes the motion of N electrons and Nn nuclei of a solid can lead only to phonon-induced superconductivity. © 1993 John Wiley & Sons, Inc.
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  • 137
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    International Journal of Quantum Chemistry 48 (1993) 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
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  • 138
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    International Journal of Quantum Chemistry 48 (1993), S. 219-224 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The energy levels in sodium atoms with quarks attached to the nucleus are obtained using the configuration interaction method. It is found that the calculated 3p (2P) → 3s (2S) electronic transition in the Na-1/3 quark-atom system is in agreement with that predicted by extrapolation of experimental data. Also, ionization potentials of fractionally charged sodium atoms are discussed. © 1993 John Wiley & Sons, Inc.
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  • 139
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    International Journal of Quantum Chemistry 48 (1993), S. 225-232 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A survey is given of the resemblance theorems associated with various types of orthonormalization procedures having different kinds of symmetry properties appearing in the current literature. It is shown that the proofs for the minimum properties are closely connected with the fact that the Hilbert-Schmidt norm of an operator is always nonnegative and has the lowest value equal to zero. © 1993 John Wiley & Sons, Inc.
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  • 140
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    International Journal of Quantum Chemistry 48 (1993), S. 233-238 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electric-field maps of certain anions and cations of adenine and guanine have been studied. The results are compared with those of neutral adenine and guanine. In all cases, the geometries were fully optimized using the MNDO molecular orbital method and the fields were computed using Mulliken charges. Reactivities and hydrogen-bonding pattern predicted by electric fields, including those of cations, are in satisfactory agreement with experiment. © 1993 John Wiley & Sons, Inc.
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  • 141
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    International Journal of Quantum Chemistry 48 (1993), S. 239-247 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this paper, a general method is presented that allows the derivation of the expansion coefficients of the product of two orthogonal functions provided the generating function is known. For the three classical orthogonal polynomials, the Laguerre, the Hermite, and the Legendre polynomials, the coefficients blmn with φmφn = ∑lblmnφl are derived. © 1993 John Wiley & Sons, Inc.
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  • 142
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    International Journal of Quantum Chemistry 48 (1993), S. 211-218 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When second-order Jahn-Teller couplings become strong along “streambeds” on potential energy surfaces, instability reflected in negative curvature along a symmetry-lowering distortion coordinate can take place. The point where such negative curvature sets in is usually not a transition state because the gradient of the potential is usually large there. In this paper, it is demonstrated how to use the local energy, local gradient, local Hessian, and knowledge of how quickly the curvature for the symmetry-breaking mode evolves along the streambed (i.e., the derivative of this curvature) to predict how far to move in the symmetry-breaking mode in search of the desired transition state. It is shown that the Hessian matrix evaluated at the symmetry-broken geometry suggested by this analysis has only one negative eigenvalue. Because this analysis is based on a local approximation to the potential, its predictions are, of course, approximate. As such, they only “suggest” the proper direction and magnitude that one should “step” to move toward a transition state. © 1993 John Wiley & Sons, Inc.
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  • 143
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    International Journal of Quantum Chemistry 48 (1993), S. 249-256 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electronegativity perturbation theory up to the fourth order has been used to study the preferred isomer of linear triatomic molecules. Systems with 10-16 valence-electron systems are discussed and our results are in good agreement with the experiment. The only exception is the isomers of PNO. The usefulness of the perturbation theory is briefly discussed. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 48 (1993), S. 257-265 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Recurrence relations are derived for the evaluation of two-electron repulsion integrals (ERIs) over Hermite and spherical Gaussian functions. Through such relations, a generic ERI or ERI derivative may be reduced to “basic” integrals, i.e., true and auxiliary integrals involving only zero angular momentum functions. Extensive use is made of differential operators, in particular, of the spherical tensor gradient Ylm(∇). Spherical Gaussians, being nonseparable in the x, y, and z coordinates, were not included in previous formulations. The advantages of using spherical Gaussians instead of Cartesian or Hermite Gaussians are briefly discussed. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 48 (1993), S. 267-276 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chain-length dependencies of 2Ag and 1Bu excitation energies as well as their unexpected inversion observed experimentally in trans-polyenes have so far been explained satisfactorily only in terms of configuration interactions within the standard Pariser-Parr-Pople (PPP) parametrization scheme with at least double excitations involving prohibitively large computational labor for long polyenes. A simpler calculation allowing nonzero differential overlap and employing restricted (first-order) single-excitation configuration interaction with chain-length-dependent screened potential is shown to provide an adequate alternative for the studies of those basic spectroscopic features of polyene excited states. The screening factor is parametrized in accordance with the chain-length-dependent behavior of the electrical polarizabilities of polyenes derived within the standard PPP approximation scheme. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 45 (1993), S. 225-225 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    International Journal of Quantum Chemistry 45 (1993), S. 189-207 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The atomic statement of the principle of stationary action determines the theorems that establish the mechanics of an atom in a molecule. The atomic torque, power, and current theorems are derived. They, along with the atomic force, virial, and continuity theorems, provide a complete description of the behavior of matter at the atomic level, including the effects of electric and magnetic fields. The atomic power theorem, for example, enables one to determine the atomic or molecular source of the creation and dissipation of power in combustion or in an explosion. An atom in a molecule is an open system and an atomic equation of motion for an observable contains a component corresponding to the flux in its current density through the atomic surface. The differential form of each theorem yields an equation of motion for the corresponding property density in which the same surface flux appears as a divergence of the current density. The differential and integrated atomic theorems complement those for the total system, enabling one to relate the property to its atomic components and ultimately to a local contribution from each element in real space. © 1993 John Wiley & Sons, Inc.
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    International Journal of Quantum Chemistry 45 (1993), S. 235-250 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In 1940, Kramers derived an expression for the rate constant of chemical reactions in viscous media. In this theory, chemical reactions are modeled as Brownian processes in the presence of potential barriers. The derivation of the rate constant is based on the solution of the Smoluchowski equation, a Fokker-Planck-type equation in position space. Kramers' theory has been confirmed for reactions in systems ranging from nuclear processes to biochemical problems. The reaction rate can be obtained from the diffusion currents appearing in the Smoluchowski equation. A Smoluchowski-type equation in position space, similar to the one applied by Kramers, has been used to find a nonlinear Schrödinger equation (NLSE) for dissipative, frictionally damped systems, taking into account wave-particle duality. For several potentials, the NLSE can be solved exactly, and analytic expressions for the currents, appearing in the Smoluchowski equation and necessary to determine the rate constants, can be obtained. These currents are not only stationary, but can also be time-dependent. It will be shown that, essentially, the determination of the time-dependence of the currents can be reduced to the solution of Newton-type equations of motion. © 1993 John Wiley & Sons, Inc.
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  • 150
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    International Journal of Quantum Chemistry 45 (1993), S. 263-294 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This paper considers a Husimi representation of quantum mechanics in which the (stationary) state of a system or ensemble is described by a Husimi function and an observable is described by a phase space function or distribution such that the expectation value of the observable is given by an integral over phase space of the product of that function or distribution and the Husimi function. The density matrix, Wigner function, and Husimi function are considered to be alternative ways of describing the state of a system or ensemble, and methods of recovering the Wigner function or density matrix from the Husimi function are discussed. The classical limits of the Wigner and Husimi functions and of the relationship between them are considered. © 1993 John Wiley & Sons, Inc.
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  • 151
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  • 152
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    International Journal of Quantum Chemistry 45 (1993), S. 333-347 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The nonlocal weighted density approximation (WDA) to the exchange and kinetic energy functionals of many-electron systems proposed several years ago by Alonso and Girifalco in the context of density functional theory is used to compute, within the framework of the spherical jellium model, the ground-state electronic density, chemical potential, and total energy of neutral and negatively and positively charged sodium clusters containing up to N = 800 atoms. From these calculations, we study the behavior of the total energies per atom, chemical potentials, ionization potentials, I(N), and electron affinities, A(N). These results are compared with analogous calculations using the well-known Thomas-Fermi-Weizsäcker-Dirac (TFWD) approximation for the kinetic (TFW) and exchange (D) energy functionals. Calculations including the local density approximation (LDA) to the correlation energy in both WDA and TFWD functionals are also presented. © 1993 John Wiley & Sons, Inc.
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  • 153
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    International Journal of Quantum Chemistry 45 (1993), S. 363-383 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We derived the necessary conditions to which the vector coupling coefficients (VCC) amn and bmn, describing atomic L, S-multiplets of pMdN and dNs1 configurations (1 ≤ N ≤ 9, 1 ≤ M ≤ 5), should satisfy. It is shown that for two-open-shell systems under consideration the unknown VCC should satisfy not only usual restrictions resulting from the spheric symmetry, but also some additional equation introduced in the present paper in the form of a postulate. VCC obtained were used for the ab initio calculations (by the general SCF coupling operator method) of several transitionmetal atoms and ions with electronic configurations 3d14p1, 3p43d3, and 3p53d3. To check the presented theory, we carried out a detailed comparison between these results and analogous data, obtained by the atomic Roothaan-Hartree-Fock method [2]. © 1993 John Wiley & Sons, Inc.
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  • 154
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    International Journal of Quantum Chemistry 45 (1993), S. 385-390 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Schrödinger equation for an atom or molecule is expressed in terms of hyperspherical coordinates. The eigenfunction is expanded in a series of orthonormal complete sets: Yλ,μ(Ω), eigenfunctions of generalized angular momentum scalar operator, and Lvn, generalized Laguerre polynomials. The recurrence relation of the expansion coefficients are derived and the eigenvalues can be obtained from the secular equation. © 1993 John Wiley & Sons, Inc.
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  • 155
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    Topics: Chemistry and Pharmacology
    Notes: We have calculated certain dynamic polarizabilities (for both real and imaginary frequencies) for H, He, and H2 and the dispersion-energy coefficients for long-range interactions between them. We have done so in a sum-over-states formalism with explicitly electron-correlated wave functions to describe the states. To be precise, we have determined the dipole (α1), quadrupole (α2), and octupole (α3) polarizabilities of H and He for real frequencies (ω) in a range between zero and the first electronic-transition frequency and for imaginary frequencies (iω) on a 32-point Gauss-Legendre grid running from zero to ħω = 20 Eh, and for H2, we have found the dipole (α), quadrupole (C), and dipole-octupole (E) polarizability tensors for the same real and imaginary frequencies. The dispersion-energy coefficients, obtained by combining the sum-over-states for-malism for the polarizabilities with analytic integration over ω, gave values of C6, C8, and C10 for the atom-atom systems; C06, C26, C08, C28, and C48 for the atom-diatom systems; and C6, C′6 and C″6 for the H2—H2 system. Nearly all the results are considered to be more reliable than those hitherto published and some have been obtained for the first time, e.g., C(iω), E(ω), and E(iω) for H2 and C08, C48, and C48 for the H—H2 system. © 1993 John Wiley & Sons, Inc.
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  • 156
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    International Journal of Quantum Chemistry 45 (1993), S. 403-403 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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  • 157
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  • 158
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    International Journal of Quantum Chemistry 45 (1993), S. 445-470 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this paper, the efficient evaluation of the atomic integrals I =∫r1ar2br3cr23λr13μr12νe-αr1-βr2-γr3dτ with one or two factors rij-2 is described. These integrals are necessary for a lower-bound calculation for Li-like systems using the method of variance minimization or Temple's formula. © 1993 John Wiley & Sons, Inc.
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  • 159
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    International Journal of Quantum Chemistry 45 (1993), S. 409-431 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Coupled-cluster equations for the calculation of the nonexpanded (fully damped) dispersion energy are derived. These equations are solved in the ring approximation using the Møller-Plesset expansion in terms of the fluctuation potentials WA and WB for the individual molecules. Numerical results of high-order perturbative calculations for the He, H2, LiH, H2O, and HF dimers are presented and compared with the converged results computed using the same basis sets. It is found that the convergence of the Møller-Plesset expansion of the dispersion energy in the ring approximation is very fast. The padé approximants still accelerate this already good convergence. For all complexes studied in this paper, the sum of the corrections through the second-order in WA + WB reproduces over 99% of the converged value. The sum of third- and higher-order corrections in the ring approximation is found to be one or two orders of magnitude smaller than the sum of second-order terms not included in the ring approximation and, therefore, may be safely neglected. Thus, it appears that a second-order calculation, which does not require iterating coupled-cluster equations or solving random phase approximation equations, offers the best compromise between accuracy and computational requirements. © 1993 John Wiley & Sons, Inc.
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  • 160
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    International Journal of Quantum Chemistry 45 (1993), S. 471-484 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The integrity bases for representations of the nuclear permutation groups Sn (n = 3,4) in the space of internal coordinates describing AXn molecules are determined. This allows optimal expressions of the molecular potential energy functions in terms of internal coordinates that are totally symmetric with respect to permutations of indistinguishable nuclei. © 1993 John Wiley & Sons, Inc.
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  • 161
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  • 162
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    International Journal of Quantum Chemistry 45 (1993), S. 491-505 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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  • 163
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    International Journal of Quantum Chemistry 45 (1993), S. 489-490 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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  • 164
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    International Journal of Quantum Chemistry 45 (1993), S. 563-572 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A p-version finite element method has been used to calculate second-order pair and total correlation energies for closed-shell Mg and Ar. Comparison with the best results found in the literature suggests that the present values are the most accurate and that the method should perform comparatively better for heavier elements. © 1993 John Wiley & Sons, Inc.
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  • 165
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    Topics: Chemistry and Pharmacology
    Notes: Some topics in relativistic quantum chemistry are reviewed with special emphasis on 4-currents and 4-potentials. It is shown that, both in molecular quantum theory and in solid-state physics, calculations can include relativistic and magnetic effects by means of 4-currents without an excessive increase in complication, provided that 4-component Dirac spinors are used rather than the Pauli approximation. © 1993 John Wiley & Sons, Inc.
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  • 166
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    International Journal of Quantum Chemistry 45 (1993), S. 587-590 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Consider two orbital sets χk, k = 1…m and η1, 1 = 1…n, which are mutually nonorthogonal. Provided that n 〉 m, at least n - m orbitals of the set {η} can be orthogonalized to the set {χ} by a transformation within the set {η}. The orthogonalization of the remaining orbitals of {η} to the set {χ} requires a transformation in which the χk appear explicitly. The orthogonalization of one orbital set to another is relevant for SCF optimizations in a truncated basis set, in the presence of frozen occupied orbitals. Examples are frozen core calculations, ECP calculations, and embedded cluster calculations, where the cluster is embedded in a frozen environment. A simple orthogonalization scheme, which makes use of a corresponding orbital transformation, is presented. It is suggested that with a small, well-defined extension of the set {η} the complete orthogonalization can be done with a transformation in which the {χ} do not appear explicitly. © 1993 John Wiley & Sons, Inc.
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  • 167
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    International Journal of Quantum Chemistry 48 (1993), S. 67-80 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ground state electron correlation is introduced into the one-particle propagator via coupled cluster theory. This defines a similarity transformation of the Hamiltonian, which leads to the complete separation of the ionization and electron attachment aspects of the propagator. The latter makes it possible to solve for each property independently. Furthermore, the frequency (or energy) dependence which characterizes propagator theory is eliminated by introducing a wave operator formalism. It is shown that this procedure is equivalent to the summation of certain types of terms in the electron propagator perturbation expansion to infinite order. Finally, the resulting equations are found to be equivalent to those of the Fock-space coupled-cluster (or equivalently the equation of motion coupled-cluster) method, which provides an explicit wave function for each state, demonstrating the connection between these different approaches for the calculation of ionization potentials and electron affinities. Understanding this relationship permits new and powerful approximations to be proposed. © 1993 John Wiley & Sons, Inc.
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  • 168
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    International Journal of Quantum Chemistry 48 (1993), S. 155-162 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 7 Tab.
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  • 169
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    International Journal of Quantum Chemistry 45 (1993), S. 71-85 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A variational principle for the transition matrix is considered. Conception of the MC SCF (in particular, CASSCF) approach for the transition matrix is proposed as a solution of the variational problem on the optimal evolution of a packet of two stationary states with some additional conditions. An ordinary MC SCF method for a single state is a special case of the proposed approach. Some aspects of the solving of the equations for the optimal transition matrix are treated. The method can be used in atomic and molecular calculations of transition energies, oscillator strengths, and other properties. © 1993 John Wiley & Sons, Inc.
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  • 170
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    International Journal of Quantum Chemistry 45 (1993), S. 105-114 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Some operators considered conventionally as Hermitian are not strictly Hermitian for the freeelectron states known especially in the case of solids. The consequences of this fact on the closure property are examined. © 1993 John Wiley & Sons, Inc.
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  • 171
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    International Journal of Quantum Chemistry 45 (1993), S. 115-117 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 172
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    International Journal of Quantum Chemistry 45 (1993), S. 123-132 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The barriers to internal rotation about the N—C bond of formamide and the formamide-H2O complex have been examined by ab initio quantum chemistry methods. Both self-consistent field and correlated approaches have been utilized to determine the geometries, energies, and local harmonic vibrational frequencies of the minimum-energy and transition-state structures of these two systems. We find that formamide's rotation barrier of 14-15 kcal/mol is increased to 16-18 kcal/mol when a single H2O molecule is attached. This result contrasts with the effect of a single H2O solvent molecule on the barrier to tautomerization of formamide (to form formamidic acid HN—CHOH) for which a barrier lowering of ca. 20 kcal/mol has been observed. The rotation barriers obtained for formamide and for its H2O complex are compared with barriers obtained experimentally in various solvents. © 1993 John Wiley & Sons, Inc.
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  • 173
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    International Journal of Quantum Chemistry 45 (1993), S. 167-176 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new formulation of the eigenvector equations for certain polymeric molecules is given. The electronic bands for the infinite molecules are deduced. For the finite molecules, the use of ghost molecules allows an exact specialization of the infinite to the finite eigenvector equations. The complete solution of the equations depends on the solution of a simple transcendental equation. Approximate solutions of this equation are given that bracket the accurate solutions so that, for molecules with many repeated moieties, the approximations become good. The general theory is illustrated by applications to the chrysene series and to the polyphenyls. © 1993 John Wiley & Sons, Inc.
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  • 174
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    International Journal of Quantum Chemistry 48 (1993), S. 269-285 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We exploit the unitary group formalism in formulating a multiconfigurational single-reference coupled cluster method for cases involving one or two electrons in open shells. The linear version of CCSD theory for the simple open shell case and for low lying singlet states of closed shell systems are considered in detail. The entire formalism is related to the unitary group based CISD method, and explicit expressions for size-extensivity corrections, leading to the L-CCSD formalism, are given. An illustrative example of the minimum basis set model of the BeH radical is also presented. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 48 (1993), S. 303-308 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This article gives an improved derivation for U(n1 + n2) ⊃ U(n1) × U(n2), SN1+N2 ⊃ SN1 × SN2, and other transformation coefficients by using a series of elementary Racah transformations. These transformation coefficients can be expressed generally in terms of a product of segments containing 6j symbols and easily calculated. Possible segment factors are given in Table I. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 48 (1993), S. 309-319 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ab initio electronic structure calculations, carried out in conjunction with rigorous analysis of the resulting wavefunctions, demonstrate that the electronic factors responsible for the unusual stability of the 1,3-dimethylimidazol-2-ylidene carbene are directly related to the substantial σ-backdonation from the carbenic carbon to the adjacent nitrogen atoms. The π-donation is found to play only a minor role, ruling out the presence of significant stabilization due to ylidic resonance structures. The unusually large proton affinity of the carbene is explained by the extra π-electron stabilization of the corresponding 1,3-dimethylimidazolium cation. The MP2/6-311++G** level of theory is found to be sufficient for accurate predictions of the geometries of the imidazol-2-ylidene carbenes. © 1993 John Wiley & Sons, Inc.
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  • 177
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    International Journal of Quantum Chemistry 48 (1993), S. 331-341 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vibration frequencies for 2-aminoethanol, neutral glycine, glycolic acid, n-propylamine, n-propanol, and propionic acid were calculated on the ab-initio RHF level with a variety of standard basis sets including polarization and diffuse functions. Experimental frequencies, if available, are compared with these data and basis set suitability is discussed on the basis of this comparison. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 48 (1993), S. 355-361 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetic energy component is shown to be a well-defined quantity in the divide-and-conquer method. This kinetic energy converges to the conventional Kohn-Sham kinetic energy when the numbers of the “buffer atoms” for subsystems increase. Numerical results from sample calculations confirm that the kinetic energy component converges to the Kohn-Sham value as the basis set increases. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 48 (1993), S. 479-490 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Results of an ab initio SCF (4-31G) study of the potential energy surface of 4-aminobutanol are reported. Four different intramolecular hydrogen bonds are present in the various local minima: N … H—O, N—H … O, C4—H … O, N … H—C1. These interactions are discussed and compared with those present in the homologues 3-aminopropanol and 2-aminoethanol. © 1993 John Wiley & Sons, Inc.
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  • 180
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    Topics: Chemistry and Pharmacology
    Notes: Many-body perturbation theory is applied to the nitrogen triple bond for bond distances ranging from the atomic regime to about 0.6a0 shorter than equilibrium. A full-optimized reaction space model is used to compute orbital spaces with an even-tempered gaussian-type basis set and also with a nominal Bagus-Gilbert Slater-type basis set. Conservation of orbital angular momentum in the atomic regime leads to perturbative theory for Hartree-Fock plus proper dissociation. Angular momentum conservation can also be enforced with a scaled Slater-Condon parameter. Third-order dissociation energies and spectroscopic constants approach limits of the chosen basis sets. © 1993 John Wiley & Sons, Inc.
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    Topics: Chemistry and Pharmacology
    Notes: The structure of 2,3-diketopiperazine in a crystal phase (P21/c), modeled by a 13-molecule cluster surrounded by point charges, was completely optimized using standard gradient procedures. The (ab initio) MIA approach was used to perform the SCF step, which using a 4-21G basis set, involves calculations using 1092 basis functions. Results are in very good agreement with experimental (X-ray) data, in contrast to a previous study in which a model was used consisting of only point charges. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 46 (1993), S. 87-100 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hartree-Fock calculations of the molecular geometry and electronic properties (ionization potentials) of bare Nin clusters (n = 3, 7, 13, and 25) and nickel clusters bearing a chemisorbed CH3 radical are reported. A basis of double-zeta quality on light atoms including carbon and a model core potential along with double-zeta plus polarization auxiliary basis set for nickel atoms have been used. Computed properties serve to assess cluster-size convergence when nickel atoms core electrons are described with [1s-3d] pseudopotentials. In spite of their simplicity, results with these potentials are in good agreement with previously reported theoretical and experimental data on seven-atom clusters. This suggests that the cluster-model approach to surface bonding using simple pseudoopotentials can lead to meaningful results and tractable computationl times when applied to larger chemisorbed organic molecules. Thus, this approach may be adequate to help find out direct experimental evidence of the interfacial bonding for grafted structures obtained under cathodic electropolymerization of acrylonitrile on nickel surfaces. © 1993 John Wiley & Sons Inc.
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  • 183
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    International Journal of Quantum Chemistry 46 (1993), S. 101-107 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: There exist problems in condensed-matter theory that require evaluating infinite Bloch sums of multipolar potential r-l-1Yl,m(θ,ϕ) on a periodic lattice. For an arbitrary multipolar order l, tractable formulas are given for summing such interactions on a two-dimensional Bravais lattice and evaluating their Bloch sums at a point outside as well as inside the plane of the lattice. The approach used is the Ewald method, which consists of separating the original series in rapidly converging sums in reciprocal and real spaces. Computational aspects of the present formulation are briefly reviewed. © 1993 John Wiley & Sons, Inc.
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  • 184
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 185
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    International Journal of Quantum Chemistry 46 (1993), S. 271-294 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Structure and the energy of the stable conformations of the two possible stereochemical configurations of 2,4-diphenylpentane are obtained using the ab initio molecular orbital theory. The objective was to mimic the possible structures and determine the corresponding energies of the dyads of syndiotactic and isotactic polystyrene and, consequently, to study the interactions between the phenyl groups. The results of complete geometry optimization showed significant changes in geometrical parameters compared with those expected from the ideal hydrocarbon structure. The steric strain is most pronounced in some of the gauche conformations where large (approximately 40°) distortions of the backbone torsional angles and/or simultaneous phenyl group rotations in the range of 30°-40° away from its global minimum position may occur. In addition to the discussion of the geometrical parameters, the corresponding dipole moments are also calculated and differences related to the various structures and discussed. © 1993 John Wiley & Sons. Inc.
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  • 186
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    International Journal of Quantum Chemistry 46 (1993), S. 319-333 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The eigenvalues of the Schrödinger equation with a polynomial potential are calculated accurately by means of the Rayleigh-Ritz variational method and a basis set of functions satisfying Dirichlet boundary conditions. The method is applied to the well potentials having one, two, and three minima. It is shown, in the entire range of coupling constants, that the basis set of trigonometric functions has the capability of yeilding the energy spectra of unbounded problems without any loss of convergence providing that the boundary value α remains greater than a critical value αcr. Only the computation of the nearly degenerate states of multiwell oscillators requires dealing with a relatively large truncation order. © 1993 John Wiley & Sons, Inc.
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  • 187
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    International Journal of Quantum Chemistry 46 (1993), S. 339-341 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 188
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    International Journal of Quantum Chemistry 46 (1993), S. 119-125 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The lowest-energy N4 is computed ab initio to be the planar C2h(3Bu) open-chain structure 13. The open-chain N4 singlet-state structures dissociate on geometry optimization. The tetraazatetrahedrane Td structure 1 and the tetrazete D2h structure 2 are minima at MP2/6-31G*. However, both are higher in energy than 13 (24.1 and 21.2 Kcal/mol [UQCISD) (T)(full)/6-311+G*//MP2/6-31G* + ZPE(MP2/6-31G)*, respectively]. The energy of 13 is 157.5 kcal/mol higher than that of two N2(1∑g+ molecules [UQCISD(T)(Full)/6-311+G*//MP2/6-31G*] © 1993 John Wiley & Sons, Inc.
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  • 189
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    International Journal of Quantum Chemistry 46 (1993), S. 671-671 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 190
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    International Journal of Quantum Chemistry 46 (1993), S. 673-674 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 191
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    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 192
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    International Journal of Quantum Chemistry 48 (1993), S. 815-826 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Many xenobiotics containing N or S heteroatoms are metabolized by the cytochrome P450s, leading to a variety of products which can be toxic, carcinogenic, or detoxifying. Thus, it is important to try to establish molecular criteria that modulate competitive product formation for these types of compounds. In the absence of 3D structures for the P450 isozymes that are responsible for the oxidations of N- and S-containing compounds, we have focused here on the characterization and identification of possible electronic and thermodynamic factors that could be modulators of different types of product formation. Specifically, the competition among N-oxidation, N-hydroxylation and Cα-hydroxylation for three amines were examined. Similarly, three thioethers were studied for their internal competition between S-oxidation and Cα-hydroxylation. The results obtained indicate that the stability of the cation radical intermediate formed by the one electron transfer mechanism is not a determinant of differences in product distribution between the two types of compounds. Rather, relative product stability appears to be a significant modulator of product distribution explaining why S-oxide formation is favored over N-oxide and why Cα-hydroxylation is usually favored over N-oxide formation in amines. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 46 (1993), S. 711-734 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This work analyses the adequacy of an analytical electrostatic energy formulation within the CNDO framework to predict the stable conformations of large molecular complexes. Comparisons are made with abinitio results for small systems such as water-formamide, methanol-water-imidazole, or guanine-cytosine and with AM1 results for two large systems: a molecular tweezer + the 9-methyladenine complex and a model active site of the α-chymotrypsin and its ligand complex. This approach is efficient in providing reliable confromers for large molecular systems in a very fast way. © 1993 John Wiley & Sons, Inc.
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  • 194
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    International Journal of Quantum Chemistry 46 (1993), S. 425-474 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We introduce a method for the explicit computation of the eigenvalue problem of the evolution operator of mixing dynamical systems. The method is based on the subdynamics decomposition of the Brussels-Austin groups directed by Professor I. Prigogine. We apply the method to three different representatives of mixing systems, namely, the Renyi maps, baker's transformations, and the Friedrichs model. The obtained spectral decompositions acquire meaning in suitable rigged Hilbert spaces that we construct explicitly for the three models. The resulting spectral decompositions show explicitly the intrinsic irreversibility of baker's transformations and Friedrichs model and the intrinsically probabilistic characters of the Renyi maps and baker's transformations. The dynamical properties are reflected in the spectrum because the eigenvalues are the powers of the Lyapunov times for the Renyi and baker systems and include the lifetimes for the Friedrichs model. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 46 (1993), S. 483-498 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new base pair (called κ-π) of Watson-Crick type, with a H-bond pattern different from that in A-T and G-C base pairs, has been recently synthesized and shown to be stable and incorporable into duplex DNA and RNA by polymerases. This new basepair, which contains three H-bonds, is compared with G-C, in the framework of modern dynamical theory of quantum nonlocality and quantum correlations. Connection with the traditional treatment of proton transfer in DNA base pairs, which uses the adiabatic approximation, is explicitly made. As a result, the dynamics of the H-bond pattern of G-C is shown to exhibit a specific quantum mechanical phase stability, which is clearly missing in the case of κ-π. This finding is discussed and illustrated, also in connection with recent quantum chemical calculations of proton transfers in DNA base pairs. Additionally, certain speculations concerning the “evolutionary advantage” of G-C with respect to κ-π are briefly considered. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 46 (1993), S. 475-481 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Band structure with a quasicontinuum of electronic states near the Fermi surface (FS) of a solid-state matter indicates overlapping regions of the electronic and phonon spectra: (εP - εQ) ≈ ℏωv. This simple fact has an important impact on the theoretical aspects of the description and a study of an electronic structure and physical properties of a matter since velocities of the nuclei and electrons are on the same scale. The motion of the electrons is not adiabatic and the description of the electronic structure of a system cannot be based on the assumption of the validity of Born-Oppenheimer approximation. For nonadiabatic systems in contrast to the descripton of adiabatic systems [(εp - εQ) 〉 ℏωv], an effect of the finite mass of the electrons, i.e.· nonadiabatic corrections, cannot be calculated by a perturbation theory due to the divergency of a perturbation expansion. Quasiparticle transformation technique has disclosed the unexpected effects of nonadiabaticity on the electronic structure and physical properties of matter. The aspects of superconductivity are discussed. © 1993 John Wiley & Sons, Inc.
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  • 197
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    International Journal of Quantum Chemistry 46 (1993) 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 198
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    International Journal of Quantum Chemistry 46 (1993), S. 499-504 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is advocated that the H-bond patterns of the standard C-G and A-T base pairs have an evolutionary advantage over any other H-bond scheme accommodated within the Watson-Crick-type geometry. A suggested proof of the statement is given by the Longuet-Higgins' sign-reversing loop argument. The present analysis indicates a close relation with self-organizational principles. © 1993 John Wiley & Sons, Inc.
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    International Journal of Quantum Chemistry 46 (1993), S. 505-510 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Some elementary properties of a general linear operator, which is defined on a Hilbert space but is not necessarily self-adjoint, are briefly reviewed: the classical canonical form, the bi-orthogonality theorem, the bivariational principle, the spectral resolution of the resolvent, and the properties of exponential forms. © 1993 John Wiley & Sons, Inc.
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  • 200
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    International Journal of Quantum Chemistry 46 (1993), S. 515-518 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Squeezed states are normally studied in configuration space or using the Glauber formalism for the coherent states. Here we show that the use of the Fock-Bargmann space can lead to more general solutions, especially in the case of squeezed states associated with the square of field amplitude. The relations that we obtain are completely general and several well-known, approximate results can be obtained as the limit cases of our approach.© 1993 John Wiley & Sons, Inc.
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