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231.
The aim of this paper was to investigate why the geometries of nonmetal hydrides are often not in accordance with the VSEPR model. From a consideration of interligand distances in a variety of BX(4), CX(4), and NX(4) molecules where X is a ligand or a lone pair and in which there are at least two H ligands we have shown that the hydrogen ligands are essentially close-packed. For each of the central atoms we have obtained a value for the ligand radius of hydrogen. These radii decrease with decreasing negative charge and increasing positive charge of the hydrogen ligand as the electronegativity of the central atom increases, as has been found previously for other ligands such as F and Cl. We show that ligand-ligand intractions are an important factor in determining bond angles in hydrides and that the ligand close-packing (LCP) model gives a better explanation of bond angles than the VSEPR model according to which bond angles depend on the electronegativity of the ligand rather than on its size. For example, although the very small angles in PH(3) and SH(2) are not in accord with the VSEPR model, they are consistent with the LCP model in that they are a consequence of the small size of hydrogen ligands which are pushed together by the lone pairs until they are almost close-packed. 相似文献
232.
Wolak MA Gillespie NB Birge RR Lees WJ 《Chemical communications (Cambridge, England)》2003,(8):992-993
A series of fluorinated cycloalkylidene indolylfulgides has been designed, synthesized and characterized; most of the thermolysis products of these fulgides maintain photochromicity and display outstanding thermal and photochemical stability. 相似文献
233.
S. E. Gillespie J. L. Oscarson R. M. Izatt P. Wang J. A. R. Renuncio C. Pando 《Journal of solution chemistry》1995,24(12):1219-1247
Flow claorimetry has been used to study the interaction of protons with glycine, DL--alanine, -alanine, DL-2-aminobutyric acid, 4-aminobutyric acid, and 6-aminocaproic acid in aqueous solutions at temperatures from 323.15 to 398.15 K. By combining the measured heats for amino acid solutions titrated with NaOH solutions with the heat of ionization for water, the log K, Ho, So, and Cp
o values for the protonation of the amino groups of these amino acids have been obtained at each temperature studied. Equations are given expressing these values as functions of temperature. The Ho and So values increase while log K values decrease as temperacture increases. The trends for log K, Ho, So, and Cp
o are discussed in terms of changes in long-range and short-range solvent effects. The trend in Ho, So, and Cp
o values with temperature and with charge separation in the zwitterions is interpreted in terms of solvent-solute interactions and the electrostatic interaction between the two oppositely charged groups within the molecule. 相似文献
234.
The bonding in a large number of hypervalent molecules of P, As, S, Se, Te, Cl, and Br with the ligands F, Cl, O, CH(3), and CH(2) has been studied using the topological analysis of the electron localization function ELF. This function partitions the electron density of a molecule into core and valence basins and further classifies valence basins according to the number of core basins with which they have a contact. The number and geometry of these basins is generally in accord with the VSEPR model. The population of each basin can be obtained by integration, and so, the total population of the valence shell of an atom can be obtained as the sum of the populations of all the valence basins which share a boundary with its core basin. It was found that the population of the V(A, X) disynaptic basin corresponding to the bond, where A is the central atom and X the ligand, varies with the electronegativity of the ligand from approximately 2.0 for a weakly electronegative ligand such as CH(3) to less than 1.0 for a ligand such as F. We find that the total population of the valence shell of a hypervalent atom may vary from close to 10 for a period 15 element and close to 12 for a group 16 element to considerably less than 8 for an electronegative ligand such as F. For example, the phosphorus atom in PF(5) has a population of 5.37 electrons in its valence shell, whereas the arsenic atom in AsMe5 has a population of 9.68 electrons in its valence shell. By definition, hypervalent atoms do not obey the Lewis octet rule. They may or may not obey a modified octet rule that has taken the place of the Lewis octet rule in many recent discussions and according to which an atom in a molecule always has fewer than 8 electrons in its valence shell. We show that the bonds in hypervalent molecules are very similar to those in corresponding nonhypervalent (Lewis octet) molecules. They are all polar bonds ranging from weakly to strongly polar depending on the electronegativity of the ligands. The term hypervalent therefore has little significance except to indicate that an atom in a molecule is forming more than four electron pair bonds. 相似文献
235.
Gillespie NB Ren L Ramos L Daniell H Dews D Utzat KA Stuart JA Buck CH Birge RR 《The journal of physical chemistry. B》2005,109(33):16142-16152
The photochemistry of the 13-desmethyl (DM) analogue of bacteriorhodopsin (BR) is examined by using spectroscopy, molecular orbital theory, and chromophore extraction followed by conformational analysis. The removal of the 13-methyl group permits the direct photochemical formation of a thermally stable, photochemically reversible state, P1(DM) (lambda(max) = 525 nm), which can be generated efficiently by exciting the resting state, bR(DM) with yellow or red light (lambda > 590 nm). Chromophore extraction analysis reveals that the retinal configuration in P1(DM) is 9-cis, identical to that of the retinal configuration in the native BR P1 state. Fourier transform infrared and Raman experiments on P1(DM) indicate an anti configuration around the C15=N bond, as would be expected of an O-state photoproduct. However, low-temperature spectroscopy and ambient, time-resolved studies indicate that the P1(DM) state forms primarily via thermal relaxation from the L(D)(DM) state. Theoretical studies on the BR binding site show that 13-dm retinal is capable of isomerizing into a 9-cis configuration with minimal steric hindrance from surrounding residues, in contrast to the native chromophore in which surrounding residues significantly obstruct the corresponding motion. Analysis of the photokinetic experiments indicates that the Arrhenius activation energy of the bR(DM) --> P1(DM) transition in 13-dm-BR is less than 0.6 kcal/mol (vs 22 +/-5 kcal/mol measured for the bR --> P (P1 and P2) reaction in 85:15 glycerol:water suspensions of wild type). Consequently, the P1(DM) state in 13-dm-BR can form directly from all-trans, 15-anti intermediates (bR(DM) and O(DM)) or all-trans, 15-syn (K(D)(DM)/L(D)(DM)) intermediates. This study demonstrates that the 13-methyl group, and its interactions with nearby binding site residues, is primarily responsible for channeling one-photon photochemical and thermal reactions and is limited to the all-trans and 13-cis species interconversions in the native protein. 相似文献
236.
Thomas Gillespie Bill M. Williams 《Journal of polymer science. Part A, Polymer chemistry》1966,4(4):933-939
Multifilm techniques have been used to measure the diffusion coefficient of water vapor in cellophane, and the data have been compared with the integral diffusion coefficient obtained in previous work with single films. The multifilm techniques lead to a much sharper resolution of the effect of concentration on diffusion, and the maximum integral diffusion coefficient. The diffusion coefficient for water vapor in cellophane peaks at a moisture content corresponding to about 70% R. H., which is presumably the “critical concentration” discussed in previous work on the thermodynamics of water sorption by cellophane. 相似文献
237.
O'Shaughnessy PN Gillespie KM Knight PD Munslow IJ Scott P 《Dalton transactions (Cambridge, England : 2003)》2004,(15):2251-2256
A group of chiral, dibasic, biaryl-bridged amido proligands containing peripheral methoxyphenyl (anisole) ligation are developed for the synthesis of new amide complexes of yttrium and lanthanum. A potentially tetradentate bis(amidoanisole) system gives, on reaction with [Y[N(SiMe(2)H)(2)](3)(THF)] a crystallographically-characterised bis complex [Y(H)] presumably as a result of low steric demand, since a more bulky version gives the target [Y[N(SiMe(2)H)(2)](THF)]. The molecular structure of the latter reveals a similar cis-alpha structure to our recently reported Schiff-base analogue. Variable-temperature NMR studies are consistent with low rigidity in the molecular structure. A potentially tridentate, amidoanisolyl/amido proligand gives complexes [M[N(SiMe(2)H)(2)](THF)(n)](M = Y, n= 1; M = La, n= 2). Chiral non-racemic versions of the above complexes were tested in the hydroamination/cyclisation of 2,2'-dimethylaminopentane to the corresponding pyrrolidine. Activities were relatively low compared to recently reported examples, and ee values were in the range 20-40% despite the well-expressed chirality of the catalysts. 相似文献
238.
239.
The VB5 interface is an ATM-based broadband interface at the V reference point, the interface between a user access and a service node (SN), also known as the SNI (service node interface) within the ITU-T. The B-ISDN architectural model allows for a number of different user accesses, such as straightforward digital sections and simple multiplexers, but it is anticipated that the most frequent implementation, particularly for mass deployment, will be via a broadband access network (AN) with VB5 interfaces.The VB5 interface is specified in a similar way to its narrowband cousin V5, in two variants – VB5.1, which supports allocation of resources via the management system, and VB5.2, which adds a mechanism for allocating AN resources under the control of the SN, enabling call-by-call concentration in the AN. This paper describes the background to the development of VB5 and explains the two variants VB5.1 and VB5.2. 相似文献
240.
Full-Wafer Characterization of AlGaN/GaN HEMTs on Free-Standing CVD Diamond Substrates 总被引:1,自引:0,他引:1
Chabak K. D. Gillespie J. K. Miller V. Crespo A. Roussos J. Trejo M. Walker D. E. Via G. D. Jessen G. H. Wasserbauer J. Faili F. Babic D. I. Francis D. Ejeckam F. 《Electron Device Letters, IEEE》2010,31(2):99-101