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Reactive scattering of Cl atoms with C2H5I molecules has been studied over the range of initial translational energy E = 63 - 24 kJ mol-1, using a supersonic beam of Cl atoms seeded in He and Ne buffer gas. Laboratory angular and velocity distributions of ICl product were measured which show that reaction proceeds via a long-lived collision complex at low initial translational energy. However at intermediate and higher initial translational energy, a forward scattered component emerges with a higher product translational energy than that of the long-lived complex component. This breakdown of long-lived complex dynamics occurs more readily in collisions at large impact parameters in contrast to the osculating complex model which assumes a statistical distribution of lifetimes independent of impact parameter.

Reactive scattering of O atoms with ICl molecules has been studied at an initial translational energy E = 40 kJ mol-1 using a supersonic beam of O atoms seeded in He and at E = 15 kJ mol-1 using O atoms seeded in Ne. Velocity distributions of OI product were measured by cross-correlation time-of-flight analysis. Full contour maps of the differential reaction cross-section have been obtained which show peaking almost equally in the forward and backward directions at both initial translational energies. The product translational energy distributions are consistent with a long-lived O-I-Cl collision complex dissociating via a loose transition state. The stability of the O-I-Cl complex is attributed to the low electronegativity of the central I atom compared with the peripheral atoms. This electronegativity ordering rule also determines the stability of the intermediates in the other reactions of oxygen atoms with halogen molecules. The mild peaking of the product angular distributions for O + ICl and IBr indicates that collision complexes have quite modest collision angular momenta L ∼ 40 ħ corresponding to impact parameters b ∼ 1·4 Å and that the angular momentum of the OI molecule in the loose transition state may be approximately half the product orbital angular momentum.

The effects of spiroxatrine, a putative antagonist with selectivity for the serotonin (5-HT)1A receptor, were compared with compounds believed to function as agonists at the 5-HT1A receptor. Schedule-controlled responding of pigeons was maintained under a multiple 30-response fixed-ratio (FR), 3-min fixed-interval (FI) schedule or under a schedule in which responding was suppressed by electric shock (“conflict” procedure). Under the multiple schedule, spiroxatrine (0.3–1.0 mg/kg) decreased FR responding but did not affect FI responding; responding was decreased in both schedule components at 3.0 mg/kg. When administered alone, buspirone, a compound believed to produce its anxiolytic effects through 5-HT1A agonist actions, produced effects similar to those of spiroxatrine; in combination, the two drugs produced greater effects than when either was administered alone. As with 5-HT1A agonists such as buspirone and 8-hydroxy-2(di-n-propylamino)tetralin (8-OH-DPAT) in the pigeon, spiroxatrine (0.01–1.0 mg/kg) increased punished responding. Spiroxatrine and buspirone were potent inhibitors of [3H]8-OH-DPAT binding to pigeon cerebral membranes with IC50 values in the nM range. Neurochemical analyses of metabolite changes produced by spiroxatrine in pigeon cerebrospinal fluid showed buspirone-like effects, with increases in MHPG, DOPAC and HVA at doses that decreased 5-HIAA levels. Spiroxatrine dose-dependently blocked the behavioral effects of the dopamine agonist piribedil indicating that, like buspirone, it also is a potent dopamine antagonist. Spiroxatrine most likely functions as an agonist at the 5-HT1A receptor. As with buspirone, however, spiroxatrine has a prominent dopamine antagonist component.

Reactive scattering of CH3 radicals with ICl, IBr, I2 and Br2 molecules has been studied at an initial translational energy E ∼ 30kJ mol-1, using a supersonic beam of CH3 radicals seeded in He buffer gas. Laboratory angular and velocity distributions of CH3I and CH3Br product have been measured which show a gradation from short-lived complex dynamics for ICl to rebound dynamics for I2 and Br2 with intermediate behaviour for IBr. This variation in dynamics is attributed to the form of the potential energy surface which shifts from a shallow hollow for CH3 + ICl to repulsion in the exit valley for CH3 + I2, Br2, with both features being present for the intermediate case of CH3 + IBr.

Reactive scattering of Cl atoms with C3H7I molecules has been studied over the range of initial translational energy E = 46-25 kJ mol-1, using a supersonic beam of Cl atoms seeded in He and Ne buffer gas. Laboratory angular and velocity distributions of ICl product were measured which show reaction proceeding via a long-lived collision complex at low initial translational energy. However a forward scattered component with a higher product translational energy appears at intermediate and higher initial translational energy. The decreased lifetimes for complexes formed in large impact parameter collisions and the high product translational energies reflect the reduced density of vibrational states prevailing for complexes with large values of the total angular momentum J ≲ 300 ħ.

Behavioral and neurochemical effects of several drugs that increase punished responding were studied in pigeons. Key pecking was established under a schedule of reinforcement in which periods of food-maintained responding alternated with periods in which behavior also was suppressed by the presentation of electric shock. Buspirone (0.1-10.0 mg/kg), gepirone (0.1-1.0 mg/kg), 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT; 0.1-3.0 mg/kg), chlordiazepoxide (3.0-30.0 mg/kg) and to a lesser extent clozapine (0.1-1.0 mg/kg) all produced increases in punished responding at doses having little effect on or decreasing the rate of unpunished responding. Neurochemical analyses on samples of cerebrospinal fluid after administration of several doses of each compound were performed for the dopamine metabolites homovanillic acid (HVA) and dihydroxyphenylacetic acid (DOPAC), the noradrenergic metabolite 3-methoxy-4-hydroxyphenylethylene glycol (MHPG) and the serotonin metabolite 5-hydroxyindoleacetic acid (5-HIAA). Gepirone, 8-OH-DPAT and the novel anxiolytic buspirone produced decreases in 5-HIAA at doses that increased punished responding in the behavioral studies. Buspirone increased levels of HVA and DOPAC, whereas its structural analog gepirone and the 5-hydroxytryptamine1A agonist 8-OH-DPAT had little effect on or decreased levels of these metabolites. Chlordiazepoxide, a prototypic benzodiazepine anxiolytic, produced only modest decreases in each of the metabolites studied. Clozapine, an atypical antipsychotic drug, produced increases in each of the metabolites studied, although only the 5-HIAA effect occurred at doses that were not behaviorally disruptive. Haloperidol (0.03-1.0 mg/kg) produced only decreases in punished and unpunished responding, whereas eliciting increases in the appearance of MHPG, DOPAC and HVA; levels of 5-HIAA were relatively unaffected.(ABSTRACT TRUNCATED AT 250 WORDS)