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  • 1985-1989
  • 1975-1979  (225)
  • 1935-1939
  • 1977  (225)
  • Atomic, Molecular and Optical Physics  (192)
  • pharmacokinetics
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 283-286 
    ISSN: 1432-1041
    Keywords: Paracetamol ; Acetaminophen ; pharmacokinetics ; first-pass elimination ; intravenous administration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Plasma paracetamol concentrations were measured in 6 volunteers after single intravenous (1000 mg) and oral (500 mg, 1000 mg and 2000 mg) doses of the drug. Paracetamol levels declined multiphasically with a mean clearance after intravenous administration of 352±40 ml/min. A two-compartment open model appeared to describe the decline adequately. Comparison of the areas under the plasma concentration-time curves (AUC) indicated that oral bioavailability increased from 0.63±0.02 after 500 mg, to 0.89±0.04 and 0.87±0.08 after 1000 mg and 2000 mg, respectively. As a consequence of the incomplete bioavailability of paracetamol, as well as its multicompartmental distribution, accurate estimates of its distribution volume and clearance cannot be obtained if the drug is given orally. However, an estimate of its total plasma clearance may be derived from the AUC after a 500 mg oral dose.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 329-335 
    ISSN: 1432-1041
    Keywords: Digoxin ; pharmacokinetics ; two-compartment model ; radioimmunoassay ; neonates ; infants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The distribution and elimination of intravenous digoxin were investigated in seven neonates and infants with heart failure. Serum digoxin concentrations during a 24 h period were determined by radioimmunoassay, using125I as tracer. The serum values declined biexponentially after the injection and could be fitted to a two-compartment open model by non-linear least-squares regression. The calculated mean half-lives of the distribution (alpha) phase in neonates and infants were 37 and 28 min, respectively. The mean half-life of the elimination (beta) phase in neonates was 44 h, as compared to 19 h in infants. The mean volume of the central compartment and the mean volume of distribution at steady-state were calculated to be 1.3 and 9.9 l/kg, respectively; no significant differences between neonates and infants were found. The relation between these volumes indicates that digoxin is extensively distributed in tissues. The steady-state distribution volumes of digoxin in neonates and infants exceed those reported in adults. The larger volume of distribution might explain in part why infants with cardiac insufficiency require larger doses of digoxin than adults (on a mg/kg body weight basis) to obtain the same serum concentrations. Elimination of digoxin from the body was slower in neonates than in infants.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 351-358 
    ISSN: 1432-1041
    Keywords: Phenprocoumon ; protein binding ; pharmacokinetics ; pharmacodynamics ; drug therapy ; myocardial infarction ; chronic disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary In nine patients, the synthesis rate Rsyn of the vitamin K-dependent clotting factors was calculated from changes in prothrombin-complex activity after intravenous administration of a synthesis-blocking dose of phenprocoumon (PPC). The biological half-life of PPC was between 2.70 and 7.01 days. No correlation was found between the level of the free fraction of this strongly protein-bound drug and its biological half-life. There was a positive correlation (p〈0.01) between the size of the free fraction of PPC and the apparent volume of distribution of the drug. Four of the patients had had an acute myocardial infarction and they showed increased sensitivity to PPC. In them the plasma level of PPC sufficient to reduce Rsyn to 50% of R°syn was significantly lower, and the depression of individual vitamin K-dependent coagulation factors was more pronounced and prolonged, than in five other patients with chronic disease. The degradation rate of coagulation factors was also found to be higher in the patients with acute myocardial infarction. In four patients with chronic disease, anticoagulant therapy with PPC was continued in the out-patient clinic. The calculated oral maintenance dose of PPC, assuming complete absorption, first-order elimination kinetics and a linear relationship between the pharmacological effect and the logarithm of the PPC-plasma concentration, showed good agreement with the dose actually found to produce the desired PP% level.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 367-375 
    ISSN: 1432-1041
    Keywords: Acenocoumarol ; excretory balance man ; pharmacokinetics ; biotransformation ; plasma protein binding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The absorption, biotransformation and elimination of the anticoagulant acenocoumarol, 3-[α- (4′-nitrophenyl)-β-acetylethyl]-4-hydroxycoumarin, have been studied by oral administration of 12 mg of a14C-labelled preparation to two male volunteers. Absorption from the gastro-intestinal tract was rapid and the plasma concentration of unchanged drug reached a maximum of 169 and 412 ng/ml, respectively, after 3 hours. The elimination half-life in the two subjects, calculated from the decline between 6 and 24 h, was 8.7 and 8.2 hours. A constant proportion of 98.7% of the drug was bound in vitro to serum proteins over a concentration range of 0.021–8.34 µg/ml, with little interindividual variation. The major portion of the binding was to human serum albumin (97.5%) at two classes of binding sites: association constant K1=1.04×105 l/mole (n1=1) and K2=5.55×103 l/mole (n2=4). In addition to unchanged acenocoumarol, four metabolites were determined in plasma by isotope dilution techniques: the amino-, acetamido-, alcohol1- and alcohol2-metabolites. Of them, the amino-metabolite showed the highest concentration, namely 278 ng/ml, after 6 h in Subject A, and 163 ng/ml after 10 hours in Subject B. Judged from the integrated concentrations, the compounds analyzed accounted for 76 and 89%, respectively, of the total radioactivity in plasma. All the metabolites detected in plasma showed anticoagulant activity when tested in mice. The quantities of the metabolites excreted in urine from 0–120 hours were (Subject A/Subject B): acenocoumarol 0.3/0.2%, amino-metabolite 12.3/7.7%, acetamido-metabolite 19.0/11.1%, alcohol1-metabolite 4.6/9.0%, alcohol2-metabolite 1.7/4.4%, 6-hydroxy-metabolite 6.9/18.3% and 7-hydroxy-metabolite 14.0/22.2%.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 51-56 
    ISSN: 1432-1041
    Keywords: Antidepressive agent ; protriptyline ; plasma concentration ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Plasma levels of protriptyline have been determined in 30 depressed female patients undergoing antidepressant therapy. After 3 1/2 weeks treatment at dosage levels of 40 mg/day, protriptyline plasma levels ranged from 430 to 1430 nmol/l. During this period only two-thirds of the subjects had definitely achieved asymptotic concentrations. Single dose studies in 5 volunteers suggest that the volume of distribution of protriptyline shows little intersubject variation. The half life of the drug, however, may vary appreciably from subject to subject, ranging from 54 to 198 h. The effects of two sedatives on mean protriptyline plasma levels have been determined. Mean plasma levels for nitrazepam recipients are indistinguishable from those for patients receiving no night sedation. The mean plasma levels for a group of patients receiving sodium amylobarbitone were significantly reduced. The problem of choice and early adjustment of dosages in order to achieve satisfactory plasma levels is discussed. For practical purposes it is suggested that early values may be of predictive significance in allowing early dosage adjustments to be made.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 473-477 
    ISSN: 1432-1041
    Keywords: Salicylate ; aspirin ; indomethacin ; pharmacokinetics ; coeliac disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The plasma concentrations of salicylate and indomethacin were measured after a single oral dose of aspirin (600 mg) and indomethacin (50 mg) in twelve starved normal subjects and twelve adult patients with coeliac disease. The absorption of salicylate in the coeliac patients was faster than in the normal subjects. The plasma concentration/time curve of indomethacin in both groups was similar during the absorption phase, but there were significant differences between the groups in its elimination. The abnormal absorption pattern of salicylate in coeliac disease does not appear to be related to its pKa. Possible causes of the difference in salicylate absorption include changes in gastric emptying or altered small intestinal permeability.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 297-303 
    ISSN: 1432-1041
    Keywords: Hydrochlorothiazide ; pharmacokinetics ; dose/response relationship ; natriuresis ; kaliuresis ; calciuresis ; magnesiuresis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Hydrochlorothiazide (hct) was administered orally in four different doses (12.5, 25, 50 and 75 mg), to eight healthy volunteers. Plasma and urine concentrations of hct were determined by GLC. Maximal plasma levels were found at 1.5–5 h, and averaged 70, 142, 260 and 376 ng × ml−1 respectively. The peak plasma levels and AUC0→9h of hct were highly correlated (p〈0.001) with the dose. The decline in the plasma curve was biphasic in those experiments in which the plasma levels of hct could be determined for at least 24 h. The half life of the slower phase lay between 5.6 and 14.8 h. The urinary recovery of hct, which represented the gastrointestinal absorption, averaged 65 to 72 per cent of the dose. The mean renal plasma clearance did not vary with the dose and averaged 319 to 345 ml × min−1. The diuresis during the 10 h after hct 12.5 mg exceeded that after placebo by a mean of 800 ml. The diureses was not increased further after higher doses of hct. The maximal natriuretic effect (+ 100 mmol), too, was found after the 12.5 mg dose. The excretion of potassium, however, rose with increasing doses; the maximal increment, after 75 mg hct, averaged 25 mmol. The excretion of calcium was significantly increased after 50 mg hct (+ 0.6 mmol). The maximal effect on magnesium excretion occurred after 25 mg hct (+ 0.5 mmol). In healthy volunteers there was no correlation between peak plasma level of hct or AUC0→9h and the renal excretion of water and electrolytes.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 305-310 
    ISSN: 1432-1041
    Keywords: Phenobarbital ; pharmacokinetics ; neonates ; infancy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary In 14 neonates 1–4 weeks old, 30 babies aged 1–12 months, and 7 infants of 1–5 years of age, the serum levels of phenobarbital were determined by a gas chromatographic micro-method after intravenous injection of phenobarbital 5–10 mg per kg body weight. It was possible to calculate the pharmacokinetic parameters using a two compartment open model. The distribution volumes within the individual age groups and the rate constants k12 and k21 showed no significant differences, but the elimination half-life was significantly longer in neonates (118.6±16.1 h) than in babies (62.9±5.2 h) or infants (68.5±3.2 h).
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  • 9
    ISSN: 1432-1041
    Keywords: Muzolimine ; pharmacodynamics ; pharmacokinetics ; furosemide ; saluresis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary In a biometrically planned, double-blind study on 12 Oedema-free male patients the saluretic effect of muzolimine 30 mg was compared with furosemide 40 mg. The plasma level of muzolimine was determined and correlated with its pharmacodynamics. In terms of excretion during the 12-hour observation period muzolimine 30 mg had as great a cumulative effect as furosemide 40 mg. There was a significant difference in the time-response curve. During the first two hours furosemide 40 mg had more saluretic effect than muzolimine 30 mg. Between two and four hours there was no significant difference between the two substances. Between four and six hours, however, muzolimine was somewhat more effective than furosemide, although the difference did not reach the level of significance. After 6 h there was no longer any difference between the two compounds. The half-life of the fall in concentration of muzolimine in plasma was 3.7 up to 10 h after its administration. The time-response curve of the increased urine excretion correlated well with the time course of the concentration of muzolimine in plasma.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 19-25 
    ISSN: 1432-1041
    Keywords: Diabetes mellitus ; sulfonylurea ; glibenclamide ; pharmacokinetics ; repeated administration ; deep compartment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Six maturity onset diabetic patients took glibenclamide 5 mg by mouth, every morning 10 min before a standard breakfast. Serum levels of immunoreactive glibenclamide, glucose and immunoreactive insulin were measured repeatedly on the first and 15th days of treatment. Measured glibenclamide blood levels were in close agreement with an analogue computer simulation of data obtained from healthy volunteers: there was no accumulation of drug in the blood, but there was strong evidence for the existence of a slowly equilibrating “deep” compartment. Considerable insulin release and correction of the breakfast-induced hyperglycaemia were observed immediately after administration of the drug, as well as 5 h later, at lunch time. The clinical significance of blood levels of glibenclamide, as well as the correlation of pharmacokinetics with pharmacodynamics, are discussed in the light of these results.
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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 117-123 
    ISSN: 1432-1041
    Keywords: Methyldopa ; radioactive label ; pharmacokinetics ; metabolism ; healthy volunteers ; intravenous and oral administration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of 2-14C-L-α-methyldopa have been investigated in five healthy volunteers following intravenous and oral administration. In the intravenous study a bi-phasic plasma concentration curve was found both for chemically determined α-methyldopa and for radioactivity. The plasma level of radioactivity differed significantly from chemically determined drug, a pattern which was also found in urine. This suggests the presence of unidentified metabolite(s). The difference between plasma disappearance and urine recovery of α-methyldopa and radioactivity during the first 4 h after injection suggests distribution to an extravascular compartment. Plasma half-lives of total radioactivity and of unchanged drug were calculated. In three subjects, pharmacokinetic parameters for a two-compartment open body model were calculated from urine and plasma data. Urinary recovery of radioactivity was almost complete within 48 h after intravenous administration. After oral administration, however, only about 40 per cent of the radioactive dose was recovered in the urine, and it contained approximately equal amounts of unconjugated methyldopa, acid-labile conjugated methyldopa and unidentified metabolite(s). The acid-labile conjugate was found only after oral administration, which supports the theory of a mucosal conjugation process. The lack of acid-labile conjugated drug either in the plasma or urine after intravenous injection indicates that there is no enterohepatic circulation of this drug.
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 355-357 
    ISSN: 1432-1041
    Keywords: Nitrazepam ; placental transfer ; pharmacokinetics ; plasma levels ; protein binding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Six women from 14 to 17 weeks pregnant, and 12 woman from 36 to 40 weeks pregnant, were given nitrazepam 5 mg orally about 12 h before legal abortion by hysterotomy in the former group and elective caesarean section in the latter group. The concentration of nitrazepam was determined by gas-liquid chromatography. Binding to plasma proteins was evaluated by separation of the protein-free fraction by ultracentrifugation. In the first group (early pregnancy) the level of nitrazepam was found to be lower in the fetal than in the maternal circulation. The concentration in amniotic fluid was still lower. In the latter group (late pregnancy) the concentration both of unbound and total nitrazepam in maternal and fetal plasma were in equilibrium, which indicated an increase in transplacental transfer in late pregnancy. The percentage of unbound nitrazepam in both cases was 12%.
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  • 13
    ISSN: 1432-1041
    Keywords: Tolmetin ; pharmacokinetics ; bioavailability ; antacid ; oral dose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The purpose of this study was to determine whether a concomitant single dose of antacid or multiple doses of antacid administered prior to, and with tolmetin, alter the pharmacokinetics of tolmetin when the drug was administered as a commercially available tablet containing tolmetin sodium. The possible effects of the antacid on plasma concentrations and urinary excretion of tolmetin and its major metabolite were evaluated following administration of: (a) tolmetin sodium alone; (b) antacid four time a day for three days prior to a single dose of tolmetin sodium, with continuation of the antacid during the day tolmetin was given; and (c) co-administration of single doses of tolmetin sodium and antacid. The twenty-four subject study was of the crossover type. There were no significant differences among treatment means for: (i) peak plasma concentrations of both tolmetin and metabolite, (ii) AUC 0–8 h and AUC 0-∞ for both tolmetin and metabolite, (iii) time to peak plasma concentration for both tolmetin and metabolite, (iv) plasma concentrations of both tolmetin and the metabolite at all sampling times (except for tolmetin at 2 h), (v) renal clearance of both tolmetin and its metabolite, and (vi) the amount of metabolite excreted in the 0–24 h urine. There were small, but significant, differences among amounts of tolmetin excreted in the 0–24 h urine. Semilogarithmic plots of both tolmetin and metabolite plasma concentrations past the peak concentrations were curved over the entire 8-h observation period; although the elimination half-life of tolmetin has been reported to be about one hour, the half-life most probably exceeds 2.6 h in most subjects. The results of this study indicate a lack of a significant drug-drug interaction between the non-steroidal anti-inflammatory agent, tolmetin sodium, and a commonly used antacid, which is a mixture of magnesium and aluminium hydroxides.
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 91-99 
    ISSN: 1432-1041
    Keywords: Disopyramide ; plasma concentration ; cardiodepressant drugs ; ventricular arrhythmia ; ventricular tachycardia ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Ten patients with various heart diseases and ventricular arrhythmia received a single oral dose of disopyramide (DE) 200 mg. The ECG was recorded continuously for about 50 h from 2–4 h before drug administration. A statistically significant reduction in the number of ventricular ectopic beats (VEBs) was seen 1.0–3.5 h after drug intake; the average number of VEBs per 30 min decreased from 317 during the control period to 92 by 1.0–3.5 h after treatment and if one patient who did not respond is excluded, the corresponding figures were 272 and 14, respectively. Consecutive VEBs were seen in seven patients before DE was given and decreased significantly (p〈0.05) 1.5–5.5 h after drug administration. There was no change in the PQ interval, the QRS interval showed a slight increase, whereas the QT interval was prolonged 0.5–4 h after administration of DE. A specific gas chromatographic method was used for DE assay in plasma and urine. Absorption was rapid in all patients. Urinary excretion during the first 48 h after drug intake varied between 35 and 75%. The lowest effective antiarrhythmic concentration estimated in six patients ranged from 1.4 to 7.0 µg/ml. β-Phase half-life in five patients was between 10.3 and 22.1 h.
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 149-154 
    ISSN: 1432-1041
    Keywords: Hydroflumethiazide ; spectrofluorometry ; pharmacokinetics ; plasma half life ; renal excretion ; renal disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary A spectrofluorometric method for determination of hydroflumethiazide in human plasma and urine has been developed. The limit of detection was 10 ng/ml plasma and 100 ng/ml urine. The plasma concentration of hydroflumethiazide was determined for 9–11 hours and excretion in urine for 24–37 hrs after oral administration of about 1 mg/kg body weight to 7 subjects. Plasma half life in healthy subjects was 1.9–2.1 h, and 2.7–8.6 h in patients during the period 4–9 hrs after dosing. Cumulative excretion in urine was 67–79% of the dose during 31–37 hrs in 6 subjects; one patient with renal disease was found to excrete only 25.8% of dose during 24 hours. Renal clearance of hydroflumethiazide was higher in the healthy subjects (0.29–0.44 1 h−1 kg−1) than in the patients (0.040–0.15 l h−1 kg−1). Plasma half life of hydroflumethiazide was not closely correlated with renal clearance of the drug, which suggests that other factors may play a role in determining plasma half life.
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 11 (1977), S. 57-64 
    ISSN: 1432-1041
    Keywords: General equation ; pharmacokinetics ; first pass effect ; extra-hepatic drug elimination
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary A general expression for the ratio of areas below the blood concentration-time curves after intravenous and oral drug administration is derived. This derivation does not require the assumption of a specific compartmental model to describe drug distribution within the body. Similarly an expression for the amount of drug metabolised in the liver is derived. The latter expression is used to estimate the extent of extra-hepatic drug elimination from the body.
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 73-76 
    ISSN: 1432-1041
    Keywords: Quinidine ; pharmacokinetics ; non-linearity ; dose-dependent pharmacokinetics ; steady state plasma level ; oral administration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Quinidine was administrated orally to five healthy male volunteers. Doses of 0.2 g t. i. d., 0.3 g t. i. d. and 0.4 g t. i. d. were given for five days with at least four weeks between each test period. The plasma concentration of quinidine was measured before the morning dose on Days 2–5 of treatment, and 1, 2, 4 and 8 h after the morning dose on the 5th day. There was not a linear relationship between the increase in dose and the increase in plasma concentration of quinidine. A dose increase of 50% from 0.6 to 0.9 g quinidine sulphate per day resulted in an increase in steady state concentration of 94%. A further 33% increase in dose, from 0.9 to 1.2 g daily, resulted in a 55% increase in the steady stae concentration of quinidine. The results demonstrate dose-dependent pharmacokinetics for quinidine. Possible explanations for the nonlinear pharmacokinetics are discussed.
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 137-145 
    ISSN: 1432-1041
    Keywords: Chlormethiazole ; pharmacokinetics ; metabolites ; oral administration ; young and elderly human subjects ; quantitative gas chromatographymass spectrometry ; whole blood distribution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The plasma concentration of chlormethiazole and two of its metabolites has been measured in three young and three aged human subjects following administration of a single oral dose of chlormethiazole. A sensitive analytical method based on gas chromatography-mass spectrometry using the selective ion monitoring mode of operation was developed to permit quantitation of the plasma levels. The time course of the plasma concentration of chlormethiazole and metabolites showed wide inter-subject variation, particularly between the young and elderly subjects. Absorption of chlormethiazole was rapid in the subjects of both groups as assessed by the time taken to reach the peak plasma concentration. The mean peak plasma level of chlormethiazole was more than five times greater in the elderly (2.90±1.56 µg/ml) than in the young (0.55±0.58 µg/ml) subjects. The plasma level of chlormethiazole was consistently higher in the aged subjects and this was reflected by the larger area under the plasma curve in aged (7.62±5.37 µg.h/ml) than in young (0.94±0.66 µg.h/ml) individuals. Decreased pre-systemic elimination by the liver has been suggested as an important factor contributing to the higher plasma level in the elderly. Estimates of absolute systemic availability, calculated by reference to previous intravenous studies, were greater for the elderly subjects. The distribution of chlormethiazole in whole blood from six young and six elderly human subjects was investigated in vitro. The unbound fraction of chlormethiazole in plasma increased significantly from 0.308±0.035 in young subjects to 0.403±0.067 in the elderly. Distribution of the drug in whole blood was different for the two age groups; the fraction of drug distributed to plasma water was significantly greater and the fraction in blood cells was significantly less in the aged.
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  • 19
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 171-174 
    ISSN: 1432-1041
    Keywords: Tolamolol ; hypertension ; pharmacokinetics ; mean steady-state concentration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Tolamolol was administered in a “double-blind” study to fifteen hypertensive patients by dose-titration against arterial blood pressure. Mean steady-state plasma tolamolol concentrations (Css) were determined for each patient from the area under the plasma concentration — time curve during a dosage interval whilst patients were receiving optimal tolamolol doses. No significant correlation was observed between daily tolamolol dose and Css; the relationship between fall in lying mean arterial pressure and Css also failed to reach conventional levels of statistical significance, but Css was observed to be correlated with the fall in standing pressure. The results suggest that plasma concentrations in excess of 200 ng/ml may be required to achieve an effective hypotensive response with the drug.
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 205-208 
    ISSN: 1432-1041
    Keywords: Cetiedil ; vasodilator ; anticholinergic drug ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Cetiedil, a new vasodilating drug with anticholinergic properties, was shown to be metabolised very rapidly in man after intravenous and oral administration of the14C-compound. Higher concentrations of labelled compound after oral than after intravenous administration at the same sampling time, and proportional differences in urinary excretion, suggest that metabolic handling of the drug differs depending on the route of administration. Experiments in which inhibition of saliva secretion was measured indicated that (an) active metabolite(s) probably was (were) responsible for the action of the drug. As an anticholinergic drug, cetiedil is at least 400 times weaker than atropine.
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  • 21
    Electronic Resource
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    Springer
    European journal of clinical pharmacology 12 (1977), S. 221-227 
    ISSN: 1432-1041
    Keywords: Cefuroxime ; cephalosporin antibiotics ; intravenous injection ; pharmacokinetics ; volunteers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Cefuroxime, a new cephalosporin antibiotic which is stable to most β-lactamases produced by Gram-negative bacteria, was given by bolus intravenous injection to six volunteers in doses of 500 mg and 750 mg. The concentrations of cefuroxime in serum and urine were measured at pre-determined times after injection and the data analysed by a two-compartment open system model. A serum concentration of 8 µg/ml was exceeded for 100.3 min (±18.3) after a 500 mg dose and for 144.5 min (±19.8) after 750 mg. The ultimate serum half-life was 1.1 h. Excretion of cefuroxime in the urine was almost complete in 24 h, the clearance being 150 ml/min/1.73 m2. About 45% was excreted through the renal tubules. The injections were well tolerated and no changes in haematological or biochemical values were seen. The resulting data are compared with those published for some other cephalosporins. It is concluded that the favourable pharmacokinetics, especially the high concentrations of unbound cefuroxime in the serum, are likely to aid effective therapy of human infection caused by sensitive bacteria.
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  • 22
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 12 (1977), S. 383-386 
    ISSN: 1432-1041
    Keywords: Benzodiazepine ; temazepam ; pharmacokinetics ; bioavailability ; hard and soft gelatine capsules
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Plasma levels of temazepam were determined in healthy subjects after single oral administration of soft and hard gelatin capsules, and after 7 consecutive night-time doses in soft capsules. Absorption from soft gelatin capsules was significantly faster and produced earlier and higher peak plasma levels. The two pharmaceutical forms did not show any significant difference in relative availability. The apparent half-life of temazepam after night-time administration was significantly shorter than after morning administration, but no change in half-life was observed between the first and seventh night-time doses.
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  • 23
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    European journal of clinical pharmacology 12 (1977), S. 125-132 
    ISSN: 1432-1041
    Keywords: Valproic acid ; pharmacokinetics ; saliva concentration ; urinary excretion ; serum protein binding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of valproic acid (VPA) have been studied in 6 healthy subjects following a single 600 mg dose, and after multiple doses over 12 days (1200 mg daily) of enteric-coated sodium valproate. A time lag before absorption of 1 to 2 h was observed in each subject, and then absorption was rapid, peak concentrations being recorded 3 to 4 h after administration of the dose. The plasma level decline was biphasic with a terminal half-life of 15.9±2.6 h in the single dose and 17.3±3.0 h in the multiple dose experiments. There was no evidence of dose dependent kinetics or autoinduction. Total plasma clearance was 0.0064±0.0011 l/kg×h. The apparent volume of distribution was small at 0.15±0.2 l/kg. The mean steady state plasma concentration (Css) reached after 4 days was 81.3±13.0 µg/ml. Css observed was lower than Css predicted (99.2±14.7 µg/ml) from single dose kinetics (p〈0.001). The difference was probably due to a reduction in plasma protein binding at higher concentrations. VPA concentration in saliva was between 0.4 and 4.5% of the total plasma concentration and was not equal to the concentration of unbound drug in plasma (6.7±0.8% unbound). 3.2% of the dose was excreted in urine as the parent drug and 21.2% as conjugated metabolites.
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  • 24
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    European journal of clinical pharmacology 12 (1977), S. 387-392 
    ISSN: 1432-1041
    Keywords: Digoxin ; β-methyldigoxin ; prolonged administration ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Five healthy volunteers received digoxin 0.4 mg or β-methyldigoxin 0.4 mg i. v., daily for 14 days, in a randomized cross-over arrangement. By monitoring minimal plasma concentrations during multiple dosing, it was found that the steady state pharmacokinetics of digoxin and β-methyldigoxin could be estimated even better by a one-compartment than by a two-compartment model. The following mean parameters were calculated: the half life of digoxin of 1.54±0.31 days was significantly shorter than the half life of 2.29±0.34 days for β-methyldigoxin. The distribution volume of 807±187 liters for digoxin was not significantly larger than the 735±227 liters for β-methyldigoxin. Renal digoxin clearance of 191±25 ml/min was significantly higher than both the renal clearance of β-methyldigoxin of 111±23 ml/min and also the creatinine clearance, which indicates tubular secretion of digoxin. There was a 2.8-fold accumulation of β-methyldigoxin injected once a day, which was significantly higher than the 1.8-fold accumulation of digoxin.
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  • 25
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    European journal of clinical pharmacology 12 (1977), S. 451-456 
    ISSN: 1432-1041
    Keywords: Bioavailability ; carbamazepine ; elimination ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The time-courses of plasma carbamazepine concentrations were followed in six apparently healthy adult subjects who, at different times, took single oral drug doses of 200, 400, 500, 600, 700, 800 and 900 mg. There were some suggestions of impaired bioavailability of the drug when given in tablet form. The following values were obtained for various pharmacokinetic parameters:k abs =0.176±0.209 h−1;k=0.0203±0.0055 h−1; T1/2=37.5±13.1 h; VD=0.825±0.1041 · kg−1; Clearance=0.0163±0.0061 l · kg−1. The elimination rate constant showed a statistically significant increase with increasing drug dose. This may help explain the clinical observation that the rate of rise of steady state plasma carbamazepine concentrations tends to decrease with dose increase in patients taking carbamazepine alone.
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  • 26
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    European journal of clinical pharmacology 12 (1977), S. 367-373 
    ISSN: 1432-1041
    Keywords: Sulphamethizole ; tetracycline ; doxycycline ; rest ; exercise ; pharmacokinetics ; excretion ; absorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The serum level and urinary excretion of sulphamethizole, tetracycline and doxycycline were studied in healthy volunteers subjected to intensive exercise and bed rest in a cross-over trial. Each group consisted of 7–8 subjects. The exercise or bed rest began 15 min before oral administration of the drug and was continued for the following 4 hours. During exercise serum drug concentration and the area under the serum concentration-time curve for each agent was significantly higher (p〈0.05) than the corresponding values at rest. Exercise greatly suppressed the renal excretion of tetracycline and doxycycline, but the decrease alone appeared insufficient to account for the pronounced increase in serum drug concentration. Total drug excretion in urine was unchanged. Thus, it seemed most unlikely that overall absorption from the gastrointestinal tract had been altered by exercise. However, the rate of absorption appeared to be more rapid in the exercise than in the rest period. Marked haemoconcentration was not produced by the exercise. In addition to changes in absorption and elimination rates, alteration in the volume of distribution might contribute to the higher serum drug concentration during exercise. Therefore, the level of physical activity should be considered in the interpretation of pharmacokinetic data both in clinical practice and in pharmacokinetic studies.
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  • 27
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    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 335-358 
    ISSN: 1573-8744
    Keywords: pharmacokinetics ; perfusion models ; sampling ; parameter estimation ; computer program ; Org GB 94 ; mianserin ; Org GC 94
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A mathematical treatment of the influence of sampling on drug kinetics in liver perfusion is presented. Based on the derived equations, a Fortran IV computer program (PERFUS) is given, by which the time course of drug concentrations can be simulated for any sampling scheme. The simulations show that the withdrawal of large samples from the reservoir, i.e., larger than 5% of the reservoir volume, results in substantially biased parameters for drugs that are rapidly distributed and/or metabolized. For the fitting of empirical data, a Fortran IV computer program is given, based on BMDX85 nonlinear least squares by Gauss-Newton iterations. This program (PERFIT) estimates model parameters corrected as if no sampling had occurred, no matter how distorted the drug disappearance curve mày be as a result of sampling or due to degeneration of the two-compartment model into a one-compartment model. The conditions under which this degeneration occurs are discussed.
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  • 28
    ISSN: 1573-8744
    Keywords: chlordiazepoxide ; benzodiazepine ; two-compartment model, biopharmaceutics ; pharmacokinetics ; single dose ; routes of administration ; intravenous ; intramuscular ; oral
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Single 30- mg doses of chlordiazepoxide HCl were administered to six healthy human subjects by the intravenous, oral, and intramuscular routes. Plasma concentration- time curves following intravenous administration were satisfactorily described by a biexponential equation consistent with a two-compartment open model system. Mean values of half-lives for the so-called distribution and elimination phases were 0.252 and 9.39 hr, respectively. The mean values for the volume of the central compartment (V 1) and volume of distribution $$(V_{d_\beta } )$$ were 18.0 and 30.9% of body weight, respectively. Following oral administration, the drug was rapidly and completely absorbed. Absorption was first order (t1/2≈27 min), and three of the six subjects showed a discernible lag time of approximately 20 min. Drug absorption following intramuscular administration was comparatively slow. A two- compartment “muscle model” comprised of precipitated and solubilized drug in the muscle was found to satisfactorily characterize the absorption process following administration by this route.
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  • 29
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    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 421-433 
    ISSN: 1573-8744
    Keywords: methotrexate ; pharmacokinetics ; model ; computer ; cancer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The infusion of high doses of methotrexate followed by folinic acid rescue is clinically useful against a variety of tumors. We studied the plasma pharmacokinetics of high-dose methotrexate infusions in patients with advanced cancer and devised a compartmental, kinetic model. our model is based on an earlier, mathematical model which describes the pharmacokinetics of moderate- to- high-dose methotrexate given as a single, intravenous injection. Mathematical equations for our model were solved on a UNIVAC1108 computer with the SAAM program. Seven compartments represent the distribution spaces for methotrexate and its metabolites. The transport of drug into and out of compartments is described by first-order differential equations. A nonlinear, concentration-dependent function is used for renal excretion with saturation of secretory and reabsorption mechanisms by methotrexate. Our model accurately depicts the pharmacokinetics of nine courses of therapy in five patients. The model can also be used to simulate the kinetics of methotrexate for patients with impaired renal function.
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  • 30
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    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 111-122 
    ISSN: 1573-8744
    Keywords: hepatic clearance ; extraction ratio ; local anesthetics ; pharmacokinetics ; lidocaine ; bupivacaine ; etidocaine ; cardiovascular effects of local anesthetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Two independent methods of calculating hepatic drug clearance were applied to data from studies of the human pharmacokinetics of lidocaine, bupivacaine, and etidocaine. Within experimental limitations, agreement was good between estimates obtained by measurement of areas under blood drug concentration-time curves after rapid intravenous injection and by direct measurement of arterial and hepatic venous drug concentrations. Apparent hepatic extraction ratios of the agents followed the order etidocaine (∼0.73)/s〉lidocaine (∼0.68〉bupivacaine (∼0.37).Pharmacokinetic implications of increases in hepatic blood flow induced by the agents are discussed.
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  • 31
    ISSN: 1573-8744
    Keywords: chlordiazepoxide ; benzodiazepine ; two-compartment model ; multiple dosing ; pharmacokinetics ; biopharmaceutics ; metabolism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Eight healthy male volunteers received chlordiazepoxide HCl orally at a dosage of 10 mg every 8 hr over a period of 21 days. On day 22, the regimen was changed to 30 mg every 24 hr for an additional 15 days. Plasma concentrations of chlordiazepoxide and its metabolites desmethyl-chlordiazepoxide, demoxepam, and desoxydemoxepam were measured during 14 of the 36 treatment days. Chlordiazepoxide plasma concentration- time data were consistent with first-order absorption and complete bioavailability. The harmonic mean absorption half-life was 12.3 min. Disposition of chlordiazepoxide was described by a two-compartment open model with a harmonic mean terminal exponential half-life of 10.1 hr. Average steady — state plasma levels of chlordiazepoxide, desmethylchlordiazepoxide, and demoxepam were approximately 0.75, 0.54, and 0.36 μg/ml, respectively.
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  • 32
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    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 513-531 
    ISSN: 1573-8744
    Keywords: pharmacokinetics ; nonlinear regression ; curve fitting ; computer program ; time sharing ; modeling ; weighting ; least squares ; parameter estimation ; discrimination between models
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The problems of curve fitting and modeling in pharmacokinetics are discussed. A new nonlinear regression program FUNFIT, written for interactive time sharing, is presented which should be more reliable than programs based on the Gauss-Newton or other related gradient methods. The new program and the well-established program NONLIN were tested on two linear models using human plasma drug level data. FUNFIT found a substantially better solution than NONLIN in the majority of the cases.
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  • 33
    ISSN: 1573-8744
    Keywords: gentamicin ; tissue distribution ; pharmacokinetics ; two-compartment modeling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Gentamicin pharmacokinetics was examined in a group of 47 patients with stable renal function treated an average of 10 days for severe infection. Serum concentrations rose continually during treatment, and declined in two phases after the drug was stopped, with a mean half-life of 112hr (range 27–693 hr) in the second phase. A two-compartment model was used to describe the biphasic decline in serum concentrations and to calculate the amount of drug in the tissue compartment at all times during and after treatment. Predicted tissue amounts of gentamicin rose continually on multiple dosing in all patients. In six patients who died, postmortem tissues were obtained to quantitate recovery. In all cases, the predicted amount of gentamicin in tissues was in close agreement with the amount recovered at autopsy. Tissue distribution and accumulation constitute a major reason for variability in gentamicin pharmacokinetics and explain both the rising peak and trough serum concentrations and the prolonged detection of gentamicin in serum and urine after the drug is stopped.
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  • 34
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    International Journal of Quantum Chemistry 11 (1977), S. 59-71 
    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 goodness of the local fit of an approximate wave-function, \documentclass{article}\pagestyle{empty}\begin{document}$ \tilde \psi $\end{document}, to the exact function, ψ0, is \documentclass{article}\pagestyle{empty}\begin{document}$ |\tilde \psi - \psi _0 | $\end{document}. From this quantity the global accuracy of \documentclass{article}\pagestyle{empty}\begin{document}$ \tilde \psi $\end{document} is defined and a “working supposition” is presented, which quantitatively relates the global accuracy to the accuracy of expectation values. Two criteria based on the accuracy of the reduced local energy and the density respectively, are presented as alternatives to \documentclass{article}\pagestyle{empty}\begin{document}$ |\tilde \psi - \psi _0 | $\end{document}. The relative global accuracies of eight wave-functions for H2 are determined using the two criteria. The ‘working supposition’ is applied and predictions are made concerning the relative accuracies of the expectation values of the following operators: z2, r2, x2 + y2, 3z2 -; r2, ξ, rA-1, r12-1, and EL (the reduced local energy). The success rate is high (〉90%) except for those operators which are sensitive to interelectron coordinates or derivatives of the wave-function.
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  • 35
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    International Journal of Quantum Chemistry 11 (1977), S. 907-916 
    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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  • 36
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    International Journal of Quantum Chemistry 11 (1977), S. 1001-1004 
    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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  • 37
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    International Journal of Quantum Chemistry 11 (1977), S. 49-57 
    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 helix-coil phase transition of DNA is studied through a model equivalent to the one used in the theory of superconductivity. A distribution function for the excitations analogous to the usual Fermi function is obtained which depends on the parameter T0, the maximum temperature at which all pairs of bases are bonded. The expression for the number of unbonded pairs of bases depends only on the two parameters, T0 and Tc (critical temperature).
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  • 38
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    International Journal of Quantum Chemistry 11 (1977), S. 103-127 
    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: Quantum mechanical tunneling theory is applied to the problem of synaptic vesicle release and to the problem of electric transmission at the ephaptic junction. In the synapse the tunneling produces conformational changes in macromolecules to open and close vesicle macrogates. Quantum mechanical tunneling as a basis for charge transfer and physical release of vesicles at junction membranes provides a unified concept of ephaptic and synaptic transmission. Details of this model are in agreement with experimental data for miniature endplate potential frequency and delay effects as a function of polarization, osmotic pressure, and temperature. The theory accounts for anatomical specializations at the synaptic cleft and the narrow junction observed for the ephapse.
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  • 39
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    International Journal of Quantum Chemistry 11 (1977), S. 187-187 
    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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  • 40
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    International Journal of Quantum Chemistry 11 (1977), S. 185-185 
    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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  • 41
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    International Journal of Quantum Chemistry 12 (1977), S. 115-131 
    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: Three simplifying methodds are discussed and applied to the four lowest valence states of CH2(3B1, 1A1, 1B1 and 1Σg+(1A1*)) and to the two lowest of CH2+(2A1 and 2∏u(2B1)). These methods concern: (1) the development of polarization functions for Gaussian-lobe basis sets by least-square fitting of numebrical multiconfigurational atomic fuinctions (this approach is tested also on (C2H2, (2) the use of intermediate Hamiltonians to calculate avoided crossings between potential hypersurfaces, and (3) thecalculation of correlation energies using an atoms-in-molecule approach.The calculated equilibrium geometries of the CH2 States are within 0.02 Å and 5° of available experimental data. The calculated term values and ionization potentials, Te(1A1 = 0.35 eV, Te (1B1) = 1.22 eV, Te (1Σg+(1A1*)) 2.48 eV, I.P. (2A1) = 10.39 eV and I. P. (2∏u(2B1)) = 10.58 eV, are in agreement with some recent theoretical studies, and are very close to existing experimental information.
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  • 42
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    International Journal of Quantum Chemistry 12 (1977), S. 193-205 
    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 focal point of our discussion is the examination of truncated basis sets used in obtaining an accurate first principles clculation of the effective valence shell Hamiltonian by the canonical transformation-cluster expansion approasch. Subsequent diagonalization of this effecitve valence shell hamiltonian yields the valence shell transition energies. A detailed analysis of numerical results obtained using a number of different basis sets of hydrogen-like orbitals together with rigorous symmetry arguments celarly demonstrates the special role played by d orbitals in computing the 3P → 1D transition energy in carbon. The failure of early attempts to calculate the effective Hamiltonian for ethylene from first principles is examined in the light of recent ab initio calculations on ethylene involving d orbitals and the computations reported in this paper. We conclude that accurate calculations of the effective valence shell Hamiltonian for molecules must consider d orbitals in the excited orbital basis set.
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  • 43
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    International Journal of Quantum Chemistry 11 (1977), S. 543-559 
    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: Quasi-relativistic (QR) versions of the CNDO and Mulliken-Wolfsberg-Helmholz (MWH) semiempirical methods based on the SCF-QR-MO-LCAO method given earlier are worked out. For the CNDO method only the basic formulas and matrix element expressions are given, while for the MWH one, the parametrization as well as the basis functions and group spinor overlap integral calculation were discussed. (PtCl6)2- complex was chosen for a test calculation. The energy level values and LCAO coefficients were obtained and compared with the nonrelativistic calculations. One of the results was the occurrence of a very strong reduction of the spin-orbit interaction due to covalency. The calculation proves the semi-empirical versions of the QR-MO-LCAO method to be quite realizable in practice.
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  • 44
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    International Journal of Quantum Chemistry 11 (1977), S. 715-723 
    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 report in this work SCF atomic calculations for Li, Be, B, C, and Ne using a basis set of completely loge-localized functions. For these second row atoms the total volume R3 was partitioned into a spherical loge of radius R and its volume complement. The loge-localized basis functions were constructed as a product of Slater-type orbitals and a cut-off factor. The energy values obtained differ significantly from the Hartree-Fock ones indicating that the delocalization effects - not included in these calculations - are important.
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  • 45
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    International Journal of Quantum Chemistry 11 (1977), S. 767-773 
    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: Gaussian orbital LCAO MO calculations are reported for pyrazine in its ground and first excited triplet state, together with calculations on its anion and cation. Energies, population analysis indices, and one-electron properties are compared across the series in order to investigate the differences in electron distribution.
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  • 46
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    International Journal of Quantum Chemistry 12 (1977), S. 759-763 
    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 spherical limit of a single particle in the field of three nuclei is shown to exhibit a variety of phenomena associated with the stability of the various extrema involved. Some consequences with respect to the general problem of detecting broken symmetry solutions of variational problems are pointed out.
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  • 47
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    International Journal of Quantum Chemistry 12 (1977), S. 737-757 
    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-body perturbation calculations have been performed for the ground state of the carbon monoxide molecule at its equilibrium internuclear separation. The calculations are complete through third order within the algebraic approximation; i.e., the state functions are parameterized by expansion in a finite basis set. All two-, three-, and four-body terms are rigorously determined, and many-body effects are found to be very important. A detailed comparison is made with a previously reported configuration interaction study. Padé approximants to the energy expansion are constructed. The many-body perturbative wave function is used in the Rayleigh quotient to produce upper bounds to the electronic energy.
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  • 48
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    International Journal of Quantum Chemistry 12 (1977), S. 765-776 
    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 effect of damping factors on convergence to general stationary solutions in many-shell SCF theory is discussed using a first order perturbation analysis. Their bearing on the maximum overlap criterion is examined and a comparison made with Hartree damping. Examples are drawn from numerical experience with hole state and transition operator calculations, some of which lead to saddle point stationary conditions. The method of Hsu et al. is reviewed in the light of the foregoing arguments.
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  • 49
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    International Journal of Quantum Chemistry 12 (1977), S. 777-779 
    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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  • 50
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    International Journal of Quantum Chemistry 12 (1977), S. 805-811 
    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 PCILO method was used to study systems with the following types of intermolecular hydrogen bonds, involving 2nd row atoms: N…H—S, S…H—S, N…H—Cl, Cl…H—F, Cl…H—Cl, P…H—N, P…H—P, P…H—F, S…H—F.In all the cases calculated, the PCILO method yields an accurate qualitative description of the stabilization energies and to some extent quantitatively good agreement with reliable ab initio and experimental results. The corresponding equilibrium distances are in almost all cases smaller (up to 0.6 Å) than the ab initio values of the same compounds.
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  • 51
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    International Journal of Quantum Chemistry 12 (1977), S. 841-850 
    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 PCILO method was used to study systematically systems with the following types of intermolecular hydrogen bonds: . In all cases the PCILO method gives a correct description of the stabilization energies in a good agreement with reliable ab initio results. The PCILO calculated equilibrium distances are only somewhat smaller than the corresponding experimental or ab initio values. Qualitatively, also, the changes in the charge distributions are in accordance with the results of ab initio calculations.
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  • 52
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    International Journal of Quantum Chemistry 12 (1977), S. 105-113 
    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: Momentum densities obtained from the Heitler-London (HL) wave functions for diatomic molecules and those from the corresponding valence-bond (VB) wave functions including ionic terms are compared. In each case they shown maxima in the direction perpendicular to the bond. However, the dependence of momentum densities on mutual orientations of the two electronic momenta is quite complex in the latter case. The improvement in the Compton profile on including the ionic terms is illustrated with the example of H2. The momentum denmsities obtained from the VB wave function constructed from orthogonalized atomic orbitals (OAO) have also been examined. The HL wave function with OAOS leads to the same momentum distribution as the repulsive state HL wave function constructed from overlapping AOS.
    Additional Material: 1 Tab.
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  • 53
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    International Journal of Quantum Chemistry 11 (1977), S. 393-398 
    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 relations between the Waller-Hartree spin-free method and the symmetric group theory are given. It is shown that the Gallup method is a special case of ours with S = M. Furthermore, all the irreducible representation matrices and other matrices needed are written explicitly in terms of Sanibel coefficients which makes the method more useful. However, it was shown that the cases with S ≠ M for the spin-free pure spin states might be beyond the power of the symmetric group theory.
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  • 54
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    International Journal of Quantum Chemistry 11 (1977), S. 381-391 
    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 quantum calculation of the optical activity and gyrotropic birefringence is used in a molecular crystal to deduce symmetry properties. A study of the variation of the components of these tensors, when a change of origin occurs, is used to account for the formula for the electric excitation proposed by Landau and Lifchitz. It is shown that the results obtained are valid in the case of crystals with nonlocalized electrons.
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  • 55
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    International Journal of Quantum Chemistry 12 (1977), S. 495-503 
    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 exact collision theory of unimolecular and bimolecular gas phase reactions is derived from a general quantum-mechanical formulation of reactions rates based on the assumption that the reactants are in thermal equilibrium. In this way the quantum corrections to the classical collision theory expressions are rigorously defined. Approximate formulas for these corrections make it possible to determine well the temperature ranges within which the classical and the semiclassical approximations are valid. A comparison is made between the collision and the transition state theory with emphasis on some conceptual difficulties of the latter in treating the simple decomposition and recombination reactions. It is shown that in the classical (high temperature) limit these theories are incompatible except when the reaction coordinate is entirely separable (i.e., when the transition state theory is no longer useful).
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  • 56
    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: Further developments of a recent semiempirical, variable effective charge MO theory for calculation of ionization potentials (IP) and electron affinities (EA) as energy differences between separately minimized ground and ionized states are reported. The method is extended to adiabatic as well as vertical IPS and EAS by including core repulsion and σ bond compression energies in the total energy. The method is generalized to heteroatomic systems and is simplified by neglecting penetration integrals. As before, only two molecular parameters, the vertical IPS of benzene and naphthalene, are required to set the magnitude of the σ changes associated with the polarization of the core during loss or gain of a π charge. Twenty-seven aromatic molecules are studied, including polyacenes, condensed ring compounds, nonbenzenoids with five and seven member rings, nonplanar molecules, and heteroatomics with N+, as in pyridine, N+2, as in pyrrole, and O+2, as in furan. The results are within 0.2 eV of the photoelectron spectroscopic vertical IPS and the predicted vertical-adiabatic separation is consistent with the shape of the first band. The calculated EAS are within 0.2 eV of the observed values.The calculation is used to predict the IP and EA of the ionic photosensitizing cyanine dye, pinacyanol. The values obtained are consistent with the latest measured IP and EA of the adsorbed dye, corrected for surface and aggregation polarization effects.
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  • 57
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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 condition for the equivalence of the Löwdin orthogonalization method and various localization methods is derived, taking the matrix elements of the localizing operator into consideration. In the example of the π atomic orbitals of benzene, it is shown that the “ultralocalized” functions defined in the Anderson fashion with help of the Boys minimum-fluctuation criterion do not fulfill this condition, in contrast with a Ruedenberg-type localization.
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  • 58
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    International Journal of Quantum Chemistry 12 (1977) 
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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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  • 59
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    International Journal of Quantum Chemistry 12 (1977), S. 671-681 
    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 method recently developed for the calculation of intramolecular nonbonded interactions based on experimental bond polarisabilities and atomic charges and transition π-charges obtained from MO calculations has been applied to the alanyl dipeptide. The potential energy contours in the φ, ψ plane obtained by this method compare favourably with those derived from the frequency of occurrence of conformations in globular proteins. An analysis of the various components of the nonbonded interaction energy indicates that the fairly frequent occurrence of conformations around φ = -80°, ψ=0° is presumably due to a favourable interaction of the π-polarisation.
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  • 60
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    International Journal of Quantum Chemistry 12 (1977), S. 549-559 
    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: Energy-shifted perturbation theory is studied in connection with corrections to Koopmans' theorem. The first three vertical Ionization potentials of N2, C2H2, and HCN are computed with basis sets of double-zeta Gaussian-type orbitals and double-zeta GTO plus polarization functions. The average absolute deviation of calculation ionization potentials from the observed values is found to be 0.4 eV, whether one uses Brillouin-Wigner or Rayleigh-Schrödinger perturbation theory.
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  • 61
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    International Journal of Quantum Chemistry 12 (1977), S. 591-591 
    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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  • 62
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    International Journal of Quantum Chemistry 12 (1977), S. 609-622 
    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: Diagrammatic many-body perturbation theory is used to calculate the potential energy function for the X1 σ+ state of the CO molecule near the equilibrium nuclear configuration. Spectroscopic constants are derived from a number of curves which are obtained from calculations taken through third order in the energy. By forming [2/1] Padé approximants to the constants we obtain: re = 1.125 Å (1.128 Å), Be = 1.943 cm-1 (1.9312 cm-1), aBe = 0.0156 cm-1 (0.0175 cm-1), We = 2247 cm-1 (2170 cm-1), WeXe = 12.16 cm-1 (13.29 cm-1), where the experimental values are given in parenthesis.
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  • 63
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    International Journal of Quantum Chemistry 12 (1977), S. 623-637 
    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: Functions of several variables, such as the electron density and the nuclear Born-Oppenheimer potential, may be analysed very effectively using orthogonal trajectories. In particular the behaviour of these trajectories at critical points of the functions is investigated in detail. The use of orthogonal trajectories in the virial partitioning of Bader and in the definition of reaction coordinates is extended. A chemical interpretation of the critical points is suggested. The relevance of catastrophe theory is illustrated.
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  • 64
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    International Journal of Quantum Chemistry 12 (1977), S. 683-705 
    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: Approximate numerical linear dependence among the columns of the two-electron integral matrix and the positiveness of the Coulomb operator are exploited in order to reduce the number of integrals that need to be calculated when a numerical accuracy is given by the machine in use or by the choice of the investigator. Numerical results presented indicate that the method leads to an algorithm for carrying out the two-electron integral four-index transformation which in practice can be achieved in a small fraction (˜1/5-1/3) of the time required to generate the integrals by one of the fastest available Gaussian integral programs, Almlöf's MOLECULE. This effectively removes one of the major bottlenecks of computational quantum chemistry.
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  • 65
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    International Journal of Quantum Chemistry 12 (1977), S. 721-735 
    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 derivation of the Born-Oppenheimer separation of electronic and nuclear motion is presented. The arguments used differ from those in earlier works in not being specially designed for molecules. Instead they aim at an intuitive understanding of the qualitative behavior of the low energy bound states of any, real or hypothetical, Coulomb interacting system of particles. The virial theorem is the starting point of the discussion. After a brief explanation of how it can be used to understand atomic structure it is applied to molecules. It is found that coordinates of collective and individual motion are natural coordinates for the approximate separation, rather than nuclear and electronic. It is also shown that it is the form of the interaction between the particles that is responsible for the separation; the smallness of met/MNu is irrelevant.
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  • 66
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    International Journal of Quantum Chemistry 12 (1977), S. 781-783 
    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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  • 67
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    International Journal of Quantum Chemistry 12 (1977), S. 785-794 
    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: Specific properties of systems with dipole-dipole interactions in the one-dimensional structures leading to the violation of the statistical equivalent of the continuity equation resulting in the creation of qualitatively new excitations are analyzed. Those excitations are the result of the interaction between the initial quasiparticle currents. The structures discussed may be of importance in biophysics, and the biophysical aspects of the obtained results are considered. In comparison with other mechanisms, the exciton mechanism is shown to be of a very specific nature as its transport properties are sharply dependent upon the type of exciting light bounded within the range of temperatures covered by living organisms. This can result in an accumulation of interface excitations on a specific lattice molecule and cause its qualitative transformations with corresponding biological consequences.
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  • 68
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    International Journal of Quantum Chemistry 12 (1977), S. 851-858 
    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: Stabilization energies and equilibrium distances of one-dimensional (HF)n and (H2O)n chains have been calculated by means of the PCILO method for finite chain length and by the PCILOCC method for infinite chain length. Both types of calculation are compared with corresponding CNDO/2-MO and CNDO/2-CO calculations. Further we have performed an analysis of the individual contributions of the stabilization energies per monomer of the PCILO and PCILOCC calculations.The results show that the PCILOCC method is well suited for the calculation of molecular associations with translational symmetry.
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  • 69
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    International Journal of Quantum Chemistry 12 (1977), S. 915-923 
    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: MO calculations of electronic structure and optical transitions for [VOn]5 -; 2n (n = 4, 5, 6) clusters in V2O5 monocrystals have been carried out by means of the semiempirical CNDO CI method. Using the calculated results, a complete analysis of V2O5 optical data as available in the literature and as obtained in the electroreflectivity experiments presented in this paper is performed. An identification of optical transitions in a wide energy range is presented. The optical properties of vanadium pentoxide are shown to be due to the localized charge transfer electronic transitions in the clusters. The fine structure of optical spectra is connected with the covalent splittings of the vanadium 3d and oxygen 2p atomic levels.
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  • 70
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    International Journal of Quantum Chemistry 12 (1977), S. 925-935 
    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 have reduced the Breit-type equation written down for 3 electrons to the 8 large components of the wave function in the (v/c)2 (Pauli) approximation. This procedure required appropriate handling of the 64 scalar equations which result in this instance. According to the results obtained within the accuracy of (v/c)2 all the terms are the same as those obtained by summing up the terms of the reduced 2-electron Breit's equation to 3 electrons. This statement is no longer valid, however, if during the reduction procedure we would go beyond the (v/c)2 approximation. Finally there is a discussion about how to begin developing a relativistic many-electron theory valid for the inner shell electrons of heavy atoms within the accuracy of the fine structure constant.
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  • 71
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    International Journal of Quantum Chemistry 12 (1977) 
    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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  • 72
    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: Reference completely ab initio 6-3G and nonempirical 3G/MODPOT (ab initio effective core model potential) LCAO-MO-SCF calculations (using the same valence atomic orbital basis) were performed for a series of boron hydrides (B4H10, B5H9, B5H11, and B6H10) and a test 3G/MODPOT + VRDDO (variable retention of diatomic differential overlap for charge conserving integral prescreening) calculation were also performed for B5H9, B6H10, and B10H14. The agreement between the ab initio 6-3G and the corresponding 3G/MODPOT calculations was excellent for valence orbital energies, gross atomic populations, and dipole moments. The results also compared favorably to previous ab initio minimum STO basis results of Lipscomb and coworkers. The 3G/MODPOT + VRDDO calculations verified that for such spatially compact molecules (such as boron hydrides, which are fragments of polyhedra), the VRDDO procedure does not result in a noticeable savings in computer time for molecules of the size and shape of B5H9 and B6H10, in contrast to the savings previously realized for organic molecules of comparable atomic size. However, the agreement in calculational results between the 3G/MODPOT and the 3G/MODPOT+VRDDO results was still as extremely close as it had been for the organic molecules.3G/MODPOT calculations were also carried out for B8H12, B9H15, B10H14, B10H14-2, 1,2-C2B4H6, and 1,6-C2B4H6 and the results compared to the previous minimum STO basis results. For B10H14, the 3G/MODPOT+VRDDO method led to savings in computer time of 28% over the 3G/MODPOT method itself.The agreement of the 3G/MODPOT results with available experimental photoelectron spectral data for B5H9 and 1,6-C2B4H6 was as good as that of the previous ab initio minimum STO basis calculations.
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  • 73
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    International Journal of Quantum Chemistry 11 (1977), S. 1-15 
    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 influence of errors in molecular integrals on the calculated RHF energy values is considered for two models which correspond to round-off and shift errors. The energy variations induced by errors in elements of one- and two-electron matrices and the overlap matrix are represented in a quadratic approximation and the same degree of accuracy is maintained for mean values and standard deviations. The formulas given point out that mean values are less than zero when some of the errors are non-shifted. Special care is required when Gaussian lobe functions are used.
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  • 74
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    International Journal of Quantum Chemistry 11 (1977), S. 17-20 
    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 derivation of most general existence conditions for surface states of a semi-infinite Kronig-Penney crystal is reported. They reduce to Steslicka's conditions under a subsidiary restriction and also indicate that the surface-state energies may lie in the allowed bulk bands. Numerical computations supporting the qualitative conclusions are provided.
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  • 75
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    International Journal of Quantum Chemistry 11 (1977), S. 325-339 
    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 recursive numerical integration scheme based on the method of Clenshaw and Curtis is proposed for the efficient implementation of the variation-iteration procedure for the computation of approximate energies and wave functions for atomic systems. Extensive numerical tests are carried out to assess the accuracy and efficiency of the method and inaccuracies in some earlier calculations are pointed out.
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  • 76
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    International Journal of Quantum Chemistry 11 (1977), S. 359-379 
    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 formalism described in the first paper of this series is applied to the chain SU(2) ⊃ D′∞ ⊃ D′4 ⊃ D′2, the covering of SO(3) ⊃ D∞ ⊃ D4 ⊃ D2. The state vectors (|αJaΓγ) adapted to each link of the chain under consideration and the corresponding coupling coefficients \documentclass{article}\pagestyle{empty}\begin{document}$ f\left( {\begin{array}{*{20}c} {J_1 } & {J_2 } & J \\ {a_1 \Gamma _1 \gamma _1 } & {a_2 \Gamma _2 \gamma _2 } & {a\Gamma \gamma } \\ \end{array}} \right) $\end{document} are given in analytical form. The material reported here is very convenient for a quantum-mechanical description of molecular and nuclear systems with linear, tetragonal, or orthorhombic symmetry. In this respect, we present an outline for its applications to the electronic and vibrational-rotational spectroscopy of molecular aggregates and to the rotational spectroscopy of molecules or nuclei. In addition, we briefly show how the material may simplify the second-order non-Lie subgroup type approach to the representation theory of SU(2).
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  • 77
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    International Journal of Quantum Chemistry 11 (1977), S. 415-425 
    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 transferability of bonds in a set of small molecules has been explored. The molecular wave-functions have been calculated from the group (or loge) function method, via a construction based on Gaussian functions. The transferability is very good and the effect of lone pairs on adjacent bonds has been analysed. Furthermore, a very simple procedure has been proposed to estimate the frontiers of the bonds.
    Additional Material: 5 Ill.
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  • 78
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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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  • 79
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    International Journal of Quantum Chemistry 11 (1977), S. 561-576 
    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 known that the 2l+1 spherical harmonics Ylm can be transformed into cyclically equivalent orbitals, of which only a few examples have so far been given explicitly. In this article the totality of such cyclic sets is derived.It is demonstrated that other kinds of equivalent spherical harmonics do not exist.Finally a set of five equivalent d orbitals related to icosahedral symmetry is introduced.
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  • 80
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    International Journal of Quantum Chemistry 12 (1977), S. 83-92 
    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 Hartree-Fock and first natural spin determinants were compared as reference determinants for calculating various one-electron properties such as ρ(0), 〈½∇〉, 〈r-2〉,…, 〈r3〉, and r-112〉. Calculations were made on various small atoms and their positive and negative ions. For nearly all the expectation values studied, the first natural spin orbital determinant gave consistently superior results. In particular, the Hartree-Fock functions gave markedly inferior results for some long range properties such as the magnentic susceptibilities of negative ions. The major correlation error in the expectation values is primarily an orbital effect which may be accounted for by including correlation terms in the one-particle Hamiltonian. Such approximate Brueckner or best overlap orbitals should reproduce most one-electron expectation values accurately.
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  • 81
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    Topics: Chemistry and Pharmacology
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    International Journal of Quantum Chemistry 11 (1977), S. 399-413 
    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 McIver-Stanton rules concerning the symmetry of transition states have a counterpart in rules concerning the permutation symmetry of single steps in degenerate rearrangements, derivable with the aid of Longuet-Higgins group theory. The generalized rules are illustrated by the widely studied PX5 polytopal rearrangements. The analysis leads to prediction of hitherto unexplored “pseudorotation” pathways for rearrangements in ethyl and homotetrahedryl cations. CNDO computations of system energies, gradients, and curvatures at critical points on the C2H5+ and C5H5+ surfaces indicate that symmetry-breaking in keeping with the permutation-theoretic predictions is a key feature of the low-energy rearrangements of these systems. In particular, computation indicates that the C2v “classical” homotetrahedral cation corresponds to an energy maximum rather than an energy minimum, or a transition state.
    Additional Material: 5 Ill.
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  • 83
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    International Journal of Quantum Chemistry 11 (1977), S. 451-472 
    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: Within the Schrödinger-Infeld-Hull factorization framework it is shown that, by introducing a parameter ε in the quantization condition, that is, ε(j-|m|)=integer ≥ 0, and, thus, considering “symmetrized” ladder operators, one can use the same formulas to handle both class I (ε = +1) and class II (ε = -1) problems. Starting from this unified point of view, after building up the associated angular momentum operators and their ε-dependent eigenfunctions, one unique closed-form expression of the coupling coefficients is obtained. This expression embodies many sparse and known previous results, without being more intricate than any of them. The basic material, allowing the application of a Wignera-Eckart theorem to matrix elements of an operator on the basis of eigenfunctions of factorizable equations, and a quick determination of the associated selection rules are given. Some examples are treated as an illustration.
    Additional Material: 3 Tab.
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  • 84
    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 formulated a pharmacological-physiological systems analysis and control theory based on interactive neuronal feedback loops (the effects of endogenous neurochemical diseases and exogenous psychotropic and other CNS drugs on neurotransmitter synthesis and release, reuptake, and metabolism) for normal, abnormal, and catastrophic situations.We were concerned primarily with the problems of stability or instability which might lead the system to exhibit catastrophic behavior. We set up the systems diagrams for the neurotransmitter systems and in that single framework were able to describe endogenous neurochemical disorders, the effect their drug treatment modalities had on the dynamic neurochemical balance, the effect psychotropic or other CNS drugs such as narcotics and narcotic antagonists had on neurotransmitter balance, and the interactive effect that multiple drug administration would have on neurotransmitter balance. Endogenous neurochemical disorders such as schizophrenia, Parkinsonism, depression, and mania should show up mathematically either as overly damped solutions if there is too little normal neurotransmitter or as catastrophically divergent instabilities if there is too much normal neurotransmitter. Improper mixed drug therapies, as well as the devastating effect of eating foods such as cheese (which contains sympathomimetic amines which potentiate the release of catecholamines from the presynaptic nerve endings) while on MAOI therapy also show up as mathematical, usually catastrophic, instabilities. We also indicated how this systems analysis and control theory could be put on small interactive computer terminals for use in clinical management and proper drug therapy of patients with neurochemical disorders.
    Additional Material: 1 Ill.
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  • 85
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    International Journal of Quantum Chemistry 12 (1977), S. 593-608 
    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: Floating spherical Gaussian orbital (FSGO) open-shell calculations have been made to determine the potential energy surface of planar square and rectangular arrangements of the four-electron system H4. This surface is discussed in relation to the bimolecular isotope exchange reaction H2+D2-→ 2HD. The changes in energy and geometry accompanying the coplanar approach of two hydrogen molecules interacting chemically have also been investigated. Calculations on the electronic energies of planar T-shaped and kite arrangements of H4 of various sizes show that it is unlikely that these configurations can serve as transition states for the exchange reaction. However, the energy curve for linear configurations of H4 (H—H—H … H), calculated as a function of the H3 … H distance with the symmetric linear H3 (H-H-H) unit fixed at the internuclear distance of 1.9080 a.u., is found to have a deep minimum (-1.9176 a.u.) at an r(H3 … H) distance of 1.5846 a.u. The overall results suggest that the following mechanism for the exchange reaction, H2+H2→H2+H+H→H3+H→H+H2+ H→H2+H2 could be advantageous as it requires a barrier height of 0.1604 a.u. which is significantly lower than that calculated from the saddle point energy (0.1950 a.u.). However, the problem of reconciling this with the experimental activation energy of 0.0685 a.u. still remains.
    Additional Material: 7 Ill.
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  • 86
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 12 (1977), S. 655-670 
    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: Excitation energies and transition moments have been determined from a second order polarization propagator and the effect of including energy shifted denominators has been investigated. Results for Be and CH+ show a change of 2-5% for the transition moments and of 0-20% for the singlet excitation energies in a second order approach compared to a first order (time-dependent Hartree-Fock) approximation. Both Be and CH+ are triplet unstable in the time-dependent Hartree-Fock approximation. The triplet instability is removed for Be but not for CH+ in a second order polarization propagator approach.
    Additional Material: 2 Ill.
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  • 87
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 11 (1977) 
    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
    Type of Medium: Electronic Resource
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  • 88
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 11 (1977), S. 21-47 
    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 full set of harmonics which are at the basis of all irreducible representations of the cubic point group and having order l ≤ 16 has been calculated in terms of Cartesian coordinates. Due to their complication, former calculations of harmonics in Cartesian coordinates for half of the irreducible representations did not exceed l = 6. The method presented in this paper is a modification of that originally given by Von der Lage and Bethe; it can be readily applied to the calculation of harmonics of arbitrary order for any irreducible representation of the cubic point group.
    Additional Material: 2 Tab.
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  • 89
    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: Following Kohn (reference 4), Schlosser and Marcus (reference 3), and Weare and Parr (reference 2), an energy functional is defined for a molecular problem which is stationary in the neighborhood of the exact solution and permits the use of trial functions that are discontinuous. The functional differs from the functional of the standard Rayleigh-Ritz method in the replacement of the usual kinetic energy operators T̂(μ) with operators T̂′(μ) = T̂(μ) + Î(μ), where Î(μ) generates contributions from surfaces of nonsmooth behavior. If one uses the ∇Ψ · ∇Ψ way of writing the usual kinetic energy contributions, one must add surface integrals of the product of the average of ∇Ψ and the change of ∇Ψ across surfaces of discontinuity.
    Additional Material: 5 Ill.
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  • 90
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    International Journal of Quantum Chemistry 11 (1977), S. 149-161 
    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 method for calculating the vertical ionization potentials and electron affinities according to their fundamental definition as differences between energies of the singlet ground and doublet ionized states is developed for cyclic hydrocarbons. The method adopts a new approach based on the central idea of a recent ab initio IP and EA calculation in which orbital exponents are optimized for both ground and ionized states. Hence, all the semi-empirical parameters of the MO theory are written as functions of the effective nuclear charge which, in turn, is made self-consistent with the molecular electronic charge distribution of the species. Although the MO theory is developed in the π electron approximation, the changes in the σ electron density, resulting from the loss or gain of a π electron, are explicitly considered in the calculation. The theory is compared to the earlier work of Hoyland and Goodman and tested against the first five polyacenes and on the condensed ring aromatics phenanthrene, pyrene, and perylene. Except for perylene, the results are in close agreement with the latest photoelectron spectroscopic measurements.
    Additional Material: 2 Ill.
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  • 91
    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 computational procedure which introduces some electron correlation into quantum mechanical calculations is described. Diverse applications are given. Among these, the method gives values of 65.6 kcal/mole for the dissociation energy of LiH, 62.0 kcal/mole for the ring-opening energy of cyclopropane, and 9.123 × 155 dynes/cm for the O-H stretching force constant of H2O. These results, and others given, suggest that our procedure has great potential and provides a very economical method for introducing electron correlation into a wave-function.
    Additional Material: 4 Ill.
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  • 92
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    International Journal of Quantum Chemistry 11 (1977), S. 277-281 
    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: Parseval's identity for orthonormal bases in Hilbert space is generalised to characterise uniquely biorthonormal bases among biorthonormal systems.
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  • 93
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    International Journal of Quantum Chemistry 11 (1977), S. 301-315 
    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 paper studies the decay, due to the spin-lattice coupling, of two ½ spins with slightly different Zeeman energies when the lattice is thermally excited. The analysis is based on obtaining, by means of the Nakajima-Zwanzig projection operator technique, an equation for the evolution of the reduced density operator of the spin system which manifests the influence of one spin on the relaxation process of the other. The zero-order solutions obtained for the evolution of the expectation values of the spin dynamics operators are essentially equivalent to the Bloch equations; higher order solutions are also obtained.
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  • 94
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    International Journal of Quantum Chemistry 11 (1977), S. 349-358 
    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 algorithm for the computation of the density of states distributions of stereoregular polymers is presented. It is related to the Gilat-Raubenheimer technique for three dimensional systems. Its application to polyethylene is briefly described.
    Additional Material: 3 Ill.
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  • 95
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    International Journal of Quantum Chemistry 11 (1977), S. 380-380 
    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
    Type of Medium: Electronic Resource
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  • 96
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    International Journal of Quantum Chemistry 11 (1977), S. 435-440 
    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 FSGO model has been used to make ab initio calculations of the geometry of B2H5+ ion. The results indicate that the acetylenic structure has the lowest energy (-43.881 a.u.) and the planar structure has the highest energy (-43.838 a.u.). The energy of the non-symmetric structure is only slightly higher (-43.879 a.u.) than that of the acetylenic one. Results of CNDO/2 calculations reported here also predict the acetylenic structure to be the most stable one.
    Additional Material: 1 Ill.
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  • 97
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    International Journal of Quantum Chemistry 11 (1977), S. 524-524 
    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
    Type of Medium: Electronic Resource
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  • 98
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    International Journal of Quantum Chemistry 12 (1977), S. 457-469 
    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 method of fractional parentage is extended to the general case of mixed configurations in arbitrary nonsimply reducible groups, G ⊂ SO(3). Particular attention is devoted to the calculation of coefficients of fractional parentage (CFP) and expressions are provided for the matrix elements of F and G type operators between N electron functions.
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  • 99
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 11 (1977), S. 441-450 
    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 series of LCAO-MO-SCF calculations, using various basis sets of Gaussian-type functions, has been made in order to study the effects of p, d, and f polarization functions for a 10-electron isoelectronic series of oxygen hydrides and for an 18-electron isoelectronic series of sulfur hydrides. Conclusions from these results suggest that meaningful proton affinities cannot be calculated without the inclusion of a d function on the heavy atom and a p function on the hydrogen atoms.
    Additional Material: 2 Ill.
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  • 100
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 11 (1977), S. 605-611 
    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 parameter optimization method of Part I is applied to the exponents of real STOS of first row atoms. In addition to minimum basis ground states, some independently optimized excited states are discussed in the case of Be. Local minima on the energy versus parameter surface are found in 4-configuration functions for the ground state of N. They are not present in either the simpler minimum basis function or in a more complete 8-configuration function.
    Additional Material: 4 Tab.
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