Molecular structure of N-chlorosuccinimide studied by gas-phase electron diffraction and quantum-chemical methods

The molecular structure of N-chlorosuccinimide has been studied by GED method at the nozzle temperature of 116 °C. Vibrational corrections to the r _a parameters, Δ(r _a − r _e), have been calculated using the scaled quadratic and cubic force constants from B3LYP/6-31G(df,p) calculations. The force field scaling has been carried out using the IR and Raman spectra of the solid N-chlorosuccinimide. The molecular skeleton and the bond conformation around nitrogen were found to be planar within large experimental errors. The equilibrium geometrical parameters derived from the experimental data assuming C _2v molecular symmetry and those from MP2(fc)/6-311G(3df,2pd) calculations are in a good agreement.     

Use of a size-consistent energy functional in many electron theory for closed shells

If the ground state wave-function ψ_gr is written as ψ_gr = Φ_o+X, withX as the correlation part satisfying (φ_o¦x) = 0, andx expressed as an expansion in terms of pair, pair-pair etc. cluster functions, then the expectation value of the energyE = (ψ_gr¦H¦ψ_gr)/(ψ_gr¦ψ_gr) has the property that the normalization term in the denominator completely cancels the unlinked part of the numerator, as noted by Sinanoglu. We use Cizek's coupled-pair ansatz ψ_gr = exp(T ₂)Φ₀ for transcribing Sinanoglu's expansion in a many-body language to study the behaviour of the size-consistent (linked) energy functional thus generated. For calculating the matrix-elements of the cluster components ofT, we use two recipes: (1) a variational determination of the cluster components using Euler's principle for the energy functional akin in spirit to the Varied Portion Approach (VPA) of Sinanoglu and (ii) a nonvariational determination of the cluster components using the conventional coupled-cluster theory. Results are presented for model test systems and are compared with variational CI and nonvariational coupled-cluster values. It has been observed that the values obtained from the size-consistent energy functional from the cluster components obtained from methods (i) and (ii) are quite close and both compare well with the nonvariational coupled-cluster results. Some useful simplifications afforded by the VPA are also indicated. A brief perspective of the method vis-a-vis other related theories is also given.     

The molecular structure of N-methylsuccinimide studied by gas-phase electron diffraction (GED) and quantum-chemical methods

The molecular structure of N-methylsuccinimide was studied by the GED method at a nozzle temperature of 69–73°C. Anharmonic vibrational corrections to thermal-average r _a bond lengths, Δ(r _a − r _e), were calculated using the quadratic and cubic force constants from B3LYP/6-31G(df, p) calculations. The molecular skeleton was found to be planar within measurement errors. Some structural effects were likely caused by the conjugation of the N atom with two C=O bonds. The equilibrium geometric parameters derived from the experimental data and those from MP2/cc-pVTZ(seg-opt) calculations were in close agreement.     

New finite-difference method for solving the pair radial equations of the many electron perturbation theory

A new convenient and efficient finite-difference (FD ) method is developed for solving the pair radial equations (PRE ) of many electron perturbation theory (MPT ). This method can be interpreted as the FD analog of the well-known Fourier method. The method is used to solve PRE arising in the second order of MPT based on the hydrogenic and Hartree–Fock (HF ) zero approximations. Being very simple programmed our method gives results comparable with the most accurate variational calculations.     

Molecular structure of 5-fluorouracil from gas-phase electron diffraction data and quantum-chemical calculations

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Molecular structure of 1,5-diazabicyclo[3.1.0]hexane as determined by gas electron diffraction and quantum-chemical calculations

The equilibrium molecular structure and conformation of 1,5-diazabicyclo[3.1.0]hexane (DABH) has been studied by the gas-phase electron-diffraction method at 20 degrees C and quantum-chemical calculations. Three possible conformations of DABH were considered: boat, chair, and twist. According to the experimental and theoretical results, DABH exists exclusively as a boat conformation of C s symmetry at the temperature of the experiment. The MP2 calculations predict the stable chair and twist conformations to be 3.8 and 49.5 kcal mol(-1) above the boat form, respectively. The most important semi-experimental geometrical parameters of DABH (r(e), A and angle)e), deg) are (N1-N5) = 1.506(13), (N1-C6) = 1.442(2), (N1-C2) = 1.469(4), (C2-C3) = 1.524(7), (C6-N1-C2) = 114.8(8), (N5-N1-C2) = 107.7(4), (N1-C2-C3) = 106.5(9), and (C2-C3-C4) = 104.0(10). The natural bond orbital (NBO) analysis has shown that the most important stabilization factor in the boat conformation is the n(N) --> sigma*(C-C) anomeric effect. The geometry calculations and NBO analysis have been performed also for the bicyclohexane molecule.     

Molecular structure of (cyanomethoxy)(dimethylamino)methane as studied by gas-phase electron diffraction and quantum-chemical calculations

The molecular structure of (cyanomethoxy)(dimethylamino)methane in the gas phase is investigated by means of gas-phase electron diffraction and quantum-chemical studies for the first time. It is shown that in the gaseous state, (cyanomethoxy)(dimethylamino)methane is a mixture of gauche-anti (65%) and anti-gauche (35%) conformers. The slight influence of the anomeric effect on the compound’s structural parameters was noted.     

Equilibrium molecular structure of orotic acid from gas-phase electron diffraction data and quantum-chemical calculations

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Vibrational and quantum-chemical study of nonlinear optical chromophores containing dithienothiophene as the electron relay

A series of nonlinear optical (NLO) donor-acceptor (D-A) chromophores containing a fused terthiophene, namely dithienothiophene (DTT), as the electron relay, the same donor group, and acceptors of various strengths, has been investigated by means of infrared and Raman spectroscopies, both in the solid state as well as in a variety of solvents, to evaluate the effectiveness of the intramolecular charge transfer from the electron-donor to the electron-acceptor end groups. The Raman spectral profiles of these NLO-phores measured from their dilute solutions have been found to be rather similar to those of the corresponding solids, and thus their intramolecular charge transfer (ICT) shows very little dependence on the solvent polarity. The experimental results obtained for the DTT-containing NLO-phore with a 4-(N,N-dibutylamino)styryl end group as the donor and a 2,2-dicyanoethen-1-yl end group as the acceptor differ from those previously obtained for two parent "push-pull" chromophores with the same D-A pair but built-up around either a bis(3,4-ethylenedioxythienyl) (BEDOT) or a bithienyl (BT) electron relay. Vibrational spectroscopy shows that DTT is significantly more efficient as an electron relay than BT (which has the same number of conjugated C=C bonds) or BEDOT (which can be viewed as a rigidified version of BT on account of noncovalent intramolecular interactions between heteroatoms of adjacent rings). Density functional theory (DFT) calculations have also been performed on these NLO-phores to assign their main electronic and vibrational features and to obtain information about their structures. An additional merit of these molecular materials was revealed by the infrared spectra of the DTT-based NLO-phores recorded at different temperatures. Thus, spectra recorded between -170 and 150 degrees C did not show any substantial change, indicating that the materials have a high thermal stability, which is of significance for their use as active components in optoelectronic devices.     

Distribution of electron density and internal rotation in phospha-alkenes according to data from quantum-chemical calculations by the MNDO method

A quantum-chemical investigation of the characteristics of the phosphorus-carbon bond and the internal rotation around it in phospha-alkenes has been carried out in the MNDO approximation. The results of the calculation have been compared with experimental dynamic ¹H NMR data.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 23, No. 6, pp. 734–736, November–December, 1987.     

A quantum-chemical and gas phase electron diffraction study of the structure of formylphosphine and acetyldimethylphosphine

The equilibrium geometry and energy and structural changes accompanying inversion motion in the phosphorus fragment and acyl group internal rotation in the H₂PCHO and Me₂PCMeO molecules were calculated by the MP2(full) method using basis sets from 6–31G(d, p) to 6–311G(3df, 2p). The structure of Me₂PCMeO was determined by electron diffraction using the dynamic model of acyl group internal rotation based on the quantum-chemical potential function of torsional motion. Acylphosphines have amide-type equilibrium conformations with acyl groups rotated through ∼100° from their orientation in the C=O/PX₂ anti- form, where X = H, Me (C ₁ symmetry). Considerable pyramidality of the phosphorus fragment distinguishes the equilibrium structures of acylphosphines from amides with a planar molecular frame (C _s symmetry). The r _h1 geometric parameters of the Me₂PCMeO molecule determined by electron diffraction closely agree with quantum-chemical estimates for the equilibrium configuration.     

Information theory and electron density

The intriguing concept of inherent uncertainty of probability schemes in information theory and statistical inference is applied to the molecular electron density. The electron density function is treated as a multimodal, three-dimensional probability density function describing the distribution of the electrons of a molecule in real space. A simple theory is proposed to introduce the amount of information associated with perturbations of the nuclear geometry such as molecular vibrations and reaction paths, in particular. It is shown by computations that the amount of information associated with the normal modes of vibration is related to the reduced mass. The proposed theory also suggests a novel Riemannian nuclear configuration space which is completely defined by the observable electron density of a molecular system.     

To the theory of electron scattering by polyatomic molecules

Within the Born-Oppenheimer adiabatic perturbation theory, an equation was obtained for the intensity of fast electron scattering by polyatomic molecules. All of its parameters are explicitly defined by vibronic interaction in a molecule; due to this, quantum chemical calculations are fully applicable to electron diffraction studies of molecular geometries. Engels Anti-Aircraft Missile Higher Military School. Translated fromZhurmal Strukturnoi Khimii, Vol. 35, No. 2, pp. 40–45, March–April, 1994. Translated by L. Smolina     

Generation of umbilics by magnets and flows

Umbilics in a nematic layer can be seen as topological defects of a complex order parameter. Being analogous to vortex lines in superfluids or superconductors, they are much easier to handle. We describe classroom experiments on controlled generation of umbilics in a nematic layer with homeotropic anchoring conditions submitted to an electric field. For this purpose we submit nematic samples to magnetic fields created by small NdFeB magnets. Umbilics induced by applied fields are unveiled by observation between crossed polarisers in monochromatic or white light. We report also on the winding action of rotating localised magnetic fields and on the winding reversal induced by Poiseuille flows.     

A quantum-chemical study of the effect of a solvent on the electron structure and reactivity of molecules

Conclusions The effect of the solvent on the electron structure and molecular reactivity has been discussed in terms of the quantum chemistry of proton transfer in a point-charge model of the NH₃+HF system.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No.1, pp.48–51, January, 1976.     

Atomic Thomas-Fermi theory and electron subshell filling

In previous work on electron subshell filling, the existence condition of the integrals involved has not been taken into proper account. As a result, part of the calculated subshell occupation numbers is meaningless. In Theis' theory [9] the average number of electrons in a subshell is calculated as the difference between two integrals. With each of these integrals an existence condition is associated. Because of this, the number of electrons with angular momentum quantum number l can only be calculated for atoms of which the Z value is (much) larger than the corresponding empirical first-appearance Z value. Thus, the range of Z for which such numbers can be calculated, is restricted considerably, especially for larger values of l. Results obtained from a normalized version of Mason's approximation [13] to the exact Thomas-Fermi function, have been compared with a least-squares fit of the empirical subshell occupation numbers, and these are found to be as good as one may expect from a statistical theory. A lower bound to each of the empirical first-appearance Z values has been calculated. The results agree well with those reported in other work.     

Phototransformation studies of halo-substituted cinnamates by Raman spectrometry and quantum-chemical computations

The comprehension of the cinnamic derivative phototransformation mechanisms is particularly important when these molecules are used as addressable photosensitive layers. In this work we show that the halo-substituted cinnamate sensitivity to the phototransformation is a function of the excitation wavelength and the substituent nature and position. With this intention, we underline the existence of various isomers and rotatomers by Raman spectroscopy and we assign the observed vibrational modes with the help of quantum-chemical calculations. These various aspects of our work clarify the relative roles of the steric, inductive and mesomeric effects according to the considered substitution.     

Photoreduction of oxoisoaporphine dyes by amines: transient-absorption and semiempirical quantum-chemical studies

Photoreduction by amines of oxoisoaporphine dyes occurs via a stepwise mechanism of electron-proton-electron transfer that leads to the metastable N-hydrogen oxoisoaporphine anion. During photoreduction that occurs from the triplet manifold of the oxoisoaporphine, a radical ion A(-)(*), a neutral-hydrogenated radical A-NH(*), and the metastable ion A-NH(-) of the oxoisoaporphine are formed. We present time-resolved spectroscopic data and quantum mechanical semiempirical PM3 and ZINDO/S results for the transient species formed during the flash photolysis of oxoisoaporphines in the presence of amines. These calculations reproduce adequately the experimental spectra of the triplet-triplet absorption near 450 nm, and that of neutral hydrogenated radical of the studied oxoisoaporphines centered at 390 nm. A transient absorption observed near 490 nm, for all of the studied systems, was explained by considering the formation of radical ion pair between the radical anion of the oxoisoaporphine, A(-)(*), and the radical cation of the amine, whose ZINDO/S calculated spectra generate the strongest transition near the experimentally observed absorption maximum at 490 nm, supporting the formation of a radical ion pair complex as the first step of the photoreduction.