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71.
The photoexcitation routes used to produce molecular crystal, triplet states are shown to have important optical and microwave spectral consequences. 2-benzoylpyridine crystals at 4.2 K have T1 → S0 phosphorescence spectra showing line width dependence on whether initial production of the T1 state is through direct T1 → S0 absorption, or through S1 ← S0 absorption followed by S1 → T1 intersystem crossing. Striking differences are seen in the optically detected zero-field resonance spectra. 相似文献
72.
The infrared (IR) spectra of cuboidic titanium carbide (TiC) nanocrystals have been studied at the density-functional-theory (DFT) level using the Becke-Perdew (BP) functional and triple-zeta quality basis sets augmented by one set of polarization functions (TZVP). The accuracy of the calculations was checked by DFT calculations using the Perdew-Burke-Ernzerhof hybrid functional (PBE0) and up to quadruple-zeta quality basis sets augmented by one set of polarization functions (QZVP). The calculated IR spectrum for Ti(14)C(13) (3 x 3 x 3) is found to be in fair agreement with the experimental IR spectrum obtained by infrared resonance-enhanced multiphoton ionization (IR-REMPI) measurements, whereas, for Ti(18)C(18) (4 x 3 x 3) and Ti(32)C(32) (4 x 4 x 4), the calculated IR spectra differ significantly from the experimental ones. The smallest TiC cluster (Ti(4)C(4), 2 x 2 x 2) considered has not been reported in any mass-spectrometer studies. The present DFT calculations show that the vibrational modes related to the in-plane vibrations of solid TiC are not observed in the IR-REMPI spectra of nanocrystals larger than Ti(14)C(13). Contrary to solid TiC, the studied TiC nanocrystals are nonmetallic with optical gaps of 0.62 eV (0.55 eV) and 0.028 eV (0.027 eV) for Ti(32)C(32) and Ti(108)C(108) (6 x 6 x 6), calculated at the time-dependent density-functional-theory (TDDFT) level using the BP functional. The HOMO-LUMO gaps obtained in the BP DFT calculations are given within parentheses. At the PBE0 DFT level, the HOMO-LUMO gaps for Ti(32)C(32) and Ti(108)C(108) are 1.74 and 0.32 eV, respectively. 相似文献
73.
This review highlights mutagenesis studies of terpene synthases, specifically sesquiterpene synthases and oxidosqualene cyclases. Mutagenesis studies of these enzymes have provided mechanistic insights, structure-function relationships for specific enzymatic residues, novel terpene structures and enzymes with novel activities. The literature through 2002 is reviewed and 113 references cited. 相似文献
74.
Cyclisation of the title compounds leads to mixtures of the expected 4H-cyclopental[b]pyrrol-4-ones (1), the corresponding 6-ones (3) by a single rearrangement, and the cyclopenta[c]pyrrol-4-ones (4) by a double rearrangement, the proportions depending upon the substituents.The 1H NMR spectra of 2-methyl-4H-cyctopenta[b]thiophen-6-one (3f) shows 6J long range coupling, but this is absent in the corresponding pyrroles (3c,d). The 13C spectra of 1 and 3 cannot be interpreted on the basis of substituent chemical shifts in pyrroles and thiophens, and are clearly -CH = CH-X (X = NMe, NPh, S) bridged derivatives of cyclopent-2-enone. 相似文献
75.
Michael C. Bhm 《International journal of quantum chemistry》1983,24(2):185-237
The validity of the Hartree–Fock (HF ) approximation in bis(π-pentadienyl)dinickel ( 1 ) and in cyclopentadienyl-allyl-cyclobutadiene-dinickel ( 2 ) has been investigated by means of the Thouless instability conditions in the computational framework of a variable model Hamiltonian. Singlet, nonsinglet (triplet), and nonreal instabilities in 1 and 2 have been studied as a function of the one-electron resonance integral β and as a function of the one- and two-center elements of the electron–electron interaction. The one-center integrals of Coulomb (γ) and exchange-type (K) have been modified by a multiplicative factor; the two-center integrals (γ) have been calculated by means of an exponential interpolation formula with a variable decay amplitude. Additionally the Thouless conditions have been studied for nuclear deformations. The stability domain of the HF solution in the model space spanned by the variable INDO Hamiltonian has been analyzed. The nature of the many-body interactions in the unstable region depends strongly on the parametrization of the model operator. HF instabilities in the high-density region (long-range forces) of 1 have their origin in individual particle–hole fluctuations while negative roots for short-range forces (low-density region) are similar to collective excitations in many-body systems (strong off-diagonal coupling). The opposite behavior is encountered in the Ni complex 2 . The physical origin of these different types of correlation processes are analyzed in a simple two-electron two-orbital model. The nature of the HF fluctuations in 1 and 2 , the importance of spatial and spin correlation, and the coupling of symmetry breaking of the electronic wave function with nuclear deformations are compared with the nature of phase transitions in solid-state systems. 相似文献
76.
A stable enzyme encapsulation technique based on the conversion of weak interactions between diazo resin/poly(styrene sulfonate) to covalent bonds was explored. Photosensitive diazoresin-based polyelectrolyte microcapsules were prepared via layer-by-layer electrostatic self-assembly of poly(styrene sulfonate) and diazoresin on MnCO(3) templates. UV-vis and zeta-potential measurements confirmed the alternate deposition of {PSS/DAR} multilayers on the micrometer-sized dissolvable templates. The DAR-based microcapsules were demonstrated to be permeable to enzymes prior to UV irradiation, while the permeability of the multilayer wall was changed substantially after photo-cross-linking. Encapsulated molecules were stably entrapped after UV irradiation, as shown by confocal microscopy and atomic force microscopy images. Activity assays revealed that encapsulated glucose oxidase possessed 52.8% of the catalytic activity exhibited by the same amount of free enzyme, proving the preservation of native conformation and accessibility of substrate. This encapsulation technique is promising for many biomedical and biotechnological applications, particularly enzyme biosensors, which require stable immobilization of functional components while allowing sufficient transport rates for substrate molecules. 相似文献
77.
Implicit solvent methods have become popular tools in the field of protein dynamics simulations, yet evaluation of their validity has been primarily limited to comparisons with experimental and theoretical data for small molecules. In this paper, we use a recently developed hybrid explicit/implicit solvent methodology to evaluate the accuracy of several Poisson-based implicit solvent models. Specifically, we focus on the calculation of electrostatic solvation free energies of various fixed conformations for two proteins. We show that, among various dielectric boundary definitions, the Lee-Richards molecular surface has the best agreement with hybrid solvent results. Furthermore, certain modifications of the molecular surface Poisson protocol provide varied results. For instance, simple modifications of atomic radii on charged residues generally improve absolute errors but do not significantly reduce relative errors among conformations. On the other hand, using a water-probe radius of 1.0 A, as opposed to the standard value of 1.4 A, to generate the molecular surface, moderately improves both absolute and relative results. 相似文献
78.
79.
MNDO calculations of heats of formation, dipole moments, ionization potentials, and structures are reported for a wide range of compounds containing chlorine in its characteristic valence state (ClI) and one or more of the elements H, B, Be, C, N, O, and F. The calculated errors in the heats of formation and the dipole moments are not significantly greater than those previously reported for compounds containing no chlorine. First vertical ionization potentials were on average 0.95 eV too high. The ordering of higher cationic states was found to be correct, even for species such as Cl2O, Cl2, and HOCl, where ab initio–Koopmans' theorem calculations predict the incorrect ordering. The calculated energies and geometries of compounds such as CIF3 are qualitatively incorrect, probably because of the lack of 3d atomic orbitals in the orbital basis set. 相似文献
80.
The kinetics of the reduction of Eu3+ and Cr3+ at mercury electrodes have been studied in various mixed perchlorate electrolytes containing iodide, bromide, and p-toluene-sulfonate as adsorbing anions. Specific adsorption data were obtained by means of the constant ionic strength approach due to Hurwitz and Parsons. The rate enhancements observed in the presence of the first two (monatomic) anions were in good agreement with the predictions of the simple Frumkin model only when the experimental, rather than calculated diffuse-layer capacitances were employed in the data analysis. It was demonstrated that the effects of ion-pairing and ligand-bridging of the reactants with the adsorbing anions were negligible under the experimental conditions chosen. From experiments with these systems and also with weakly adsorbing chloride electrolytes it was concluded that ion-pairing did not enhance the electrochemical reactivity of either Eu3+ or Cr3+. The value of the analyses described in separating various contributions to the catalytic effects of adsorbing anions is emphasized. 相似文献