8-甲氧基呋喃并[3′,2′:6,7]香豆素与烯烃的光环合加成反应的量子化学研究

我们用CNDO/Ⅱ方法UI对四甲基乙烯,偏甲基乙氧基乙烯,三甲基乙烯和丙烯睛等四个烯烃分子作了量子化学计算,它们的几何参数均采用pople标准数据。     

A computationally efficient and reliable bond order measure

Bond order indexes are useful measures that connect quantum mechanical results with chemical understanding. One of these measures, the natural bond order index, based on the natural resonance theory procedure and part of the natural bond orbital analysis tools, has been proved to yield reliable results for many systems. The procedure's computational requirements, nevertheless, scales so highly with the number of functions in the basis set and the delocalization of the system, that the calculation of this bond order is limited to small or medium size molecules. We present in this work a bond order index, the first order perturbation theory bond order (fopBO), which is based on and strongly connected to the natural bond orbital analysis tools. We present the methodology for the calculation of the fopBO index and a number of test calculations that shows that it is as reliable as the natural bond orbital index, with the same weak sensitivity to variations among commonly used basis sets and, as opposed to the natural bond order index, suitable for the study of large systems, such as most of those of biological interest.     

Comparison of the AIM delocalization index and the Mayer and fuzzy atom bond orders

In this paper the behavior of three well-known electron-sharing indexes, namely, the AIM delocalization index and the Mayer and fuzzy atom bond orders are studied at the Hartree-Fock level. A large number of five-membered ring molecules, containing several types of bonding, constitute the training set chosen for such purpose. A detailed analysis of the results obtained shows that the three indexes studied exhibit strong correlations, especially for homonuclear bonds. The correlation is somewhat poorer but still significant for polar bonds. In this case, the bond orders obtained with the Mayer and fuzzy atom approaches are normally closer to the formally predicted bond orders than those given by the AIM delocalization indexes, which are usually smaller than those expected from chemical intuition. In some particular cases, the use of diffuse functions in the calculation of Mayer bond orders leads to unrealistic results. In particular, noticeable trends are found for C-C bonds, encouraging the substitution of the delocalization index by the cheaper fuzzy atom or even the Mayer bond orders in the calculation of aromaticity indexes based on the delocalization index such as the para-delocalization index and the aromatic fluctuation index.     

Electron delocalization and bond formation under the ELF framework

A first approach to the relationship between the electron localization function (ELF) and electronic delocalization upon bond formation is provided. We show from first principles the ability of ELF at the bond critical points to act as an index of the electron reorganization involved in chemical bonding. Simultaneously, this index, that we shall call ELF delocalization index (EDI), constitutes a good measure of electron delocalization. We will show how the core of ELF is proportional to the Wiberg index under the valence bond approach. This relationship will be exploited for some representative examples where EDI is able to identify the stages of bond formation. Furthermore, a maximum in EDI along this process has been found to correlate with the molecular equilibrium configuration, allowing for a formulation of a ??maximal localization principle?? for the stable structure of covalent compounds in terms of ELF.     

Definition of an isodesmicity index from G3B3 energy components

In this work, we define an isodesmicity index, which allows the evaluation of the conservation of the error within a given bond conserving reaction. This index is reaction‐specific and, therefore, does not rely on the nature of the reference systems. Several aspects of the index are tested, to verify that this measurement shows the desired behavior. The index is a tool, which should allow the user to establish the “best” bond conserving process for, for instance, the determination of a heat of formation. © 2011 Wiley Periodicals, Inc. Int J Quantum Chem, 2012     

Bond indices and heats of formation of some nitriles

The definition of bond index introduced by Ehrenson, and written in terms of bond order and overlap integrals, has been applied to a series of nitriles. A good correlation between heats of formation and a linear equation in the indices for each bond present is obtained. This was extended to include the results for a set of hydrocarbons.     

About counterintuitive orbital mixing and bond populations

It is shown that negative bond and orbital populations may be avoided by the introduction of a weight factor in a bond index definition, together with a suitable parameterization. The negative bond populations found for first-row metal complexes need not be ascribed to counterintuitive orbital mixing but rather, essentially, to the equipartition of the charge distribution. Different definitions of the bond population are compared for ferrocene and the effects of some parameterizations are discussed.     

How H-bonding affects aromaticity of the ring in variously substituted phenol complexes with bases. 4. Molecular geometry as a source of chemical information

Aromaticity of the ring of variously substituted phenols in their H-bonded complexes with various bases was a subject of analysis based on 664 geometries retrieved from CSD and by use of the aromaticity index HOMA. GEO and EN, the components of the HOMA index, describing a decrease of aromaticity due to an increase of bond alternation (GEO term) and bond elongation (EN term), were also studied. There is an approximate monotonic dependence of HOMA and GEO on the H-bond strength estimated by the C-O bond length of the hydroxyl group in phenols.     

Topological analysis of the electron localisation function (ELF) applied to the electronic structure of oxaziridine: the nature of N-O bond

Structural Chemistry - Topological analysis of the electron localisation function (ELF), natural bond orbital and Wiberg bond index calculations have been applied to study the electronic structure...     

Impersonality of the connectivity index and recomposition of topological indices according to different properties

The connectivity index chi can be regarded as the sum of bond contributions. In this article, boiling point (bp)-oriented contributions for each kind of bond are obtained by decomposing the connectivity indices into ten connectivity character bases and then doing a linear regression between bps and the bases. From the comparison of bp-oriented contributions with the contributions assigned by chi, it can be found that they are very similar in percentage, i.e. the relative importance of each particular kind of bond is nearly the same in the two forms of combinations (one is obtained from the regression with boiling point, and the other is decided by the constructor of the chi index). This coincidence shows an impersonality of chi on bond weighting and may provide us another interpretation of the efficiency of the connectivity index on many quantitative structure-activity/property relationship (QSAR or QSPR) results. However, we also found that chi's weighting formula may not be appropriate for some other properties. In fact, there is no universal weighting formula appropriate for all properties/activities. Recomposition of some topological indices by adjusting the weights upon character bases according to different properties/activities is suggested. This idea of recomposition is applied to the first Zagreb group index M(1) and a large improvement has been achieved.     

Nature of bonding in the sulfuryl group

The SO sulfuryl bond in a number of representative sulfoxides and sulfones has been studied at the B3LYP/6-311+G(d,p) level in the atoms-in-molecules (AIM) approach involving the AIM delocalization index and the Cioslowski-Mixon localized orbitals and associated covalent bond order. The sulfur-oxygen covalent bond is strongly polarized toward oxygen and the oxygen lone pairs provide significant backbonding to create short and strong SO bonds, similar in nature to those found in the analogous phosphoryl (PO) bond. Although the sulfoxides in general have larger delocalization indices than the sulfones, there is no correlation between these quantities and the bond dissociation energies.     

一个新的拓扑指数用于有机化合物的QSPR/QSAR研究

在分子图的邻接矩阵和距离矩阵的基础上提出了一个新的拓扑指数Xu,该拓扑指数易于计算,对C~2-C~1~6饱和烷烃有较高的结构区分能力,通过适当的处理可方便地推广到含多重键杂原子体系。该指数与饱和烷烃的正常沸点等理化性质,不饱和链烃类化合物的热容以及某些脂肪醇的毒性和疏水性参数均具有较好的性质相关性。绝大多数理化性质与Xu指数均能建立简单线性模型,且相关系数均大于0.99,表明该指数有望在QSPR/QSAR研究中作为一个新的参数而获得推广应用。     

Chemical Bond Parameters in Sr_3MRhO_6(M=Rare earth)

over tile years, tile collcept of bolld covalellcy or ionicity has been proved to be a veryilllpol'tallt quantity in classifyillg and explaining many basic properties of molecules andsolids from the viewpoint of the electronic structure. Nevertheless, previous study in thisaspect was only on binary crystals, which limited the usefulness of the theory. Therecently proposed method I for the evaluation of chemical bond parameters includingbond covalency has made the study on crystals with multipl…     

The use of bond paths for quantitatively characterizing bond strain

The concept of the bond path as a means for characterizing individual strained bonds is developed in detail and applied to a variety of molecules. A reference path is defined in terms of the superposed electronic densities of the free atoms, and a “bond deviation index” is introduced, for expressing quantitatively the difference between the actual and the reference bond paths. This difference is taken as indicating the degree of strain in the bond. It is shown that bond paths can be significantly affected by not only neighboring bonding electrons, but by lone pairs as well, as in the H₂O and NH₃ molecules.     

Bond Fukui functions as descriptor of the electron density reorganization in π conjugated systems

The bond Fukui function is introduced and tested as a new reactivity index capable of predicting the evolution of bond breaking and formation processes during an organic reaction involving π conjugated systems. As an illustration, we examine many cases where substituted ethylenes and dienes may respond to different reagents to yield cycloaddition, Michael addition, and other reactions at double bonds.     

ZSM-5分子筛生成中的模板效应Ⅵ.常用模板剂模板指数的测定

在定义模板指数概念的基础上,测定了7种常用模板剂的模板指数,并对模板指数表征模板效应强弱的可信性给以验证。结果表明模板指数所表示的模板剂的模板效应的强弱次序与实验结果一致,也与前人工作的定性结果一致。从而提出了用简单方法定量评价和选择ZSM-5分子筛模板剂的新途径。     

Electronic structures, intramolecular interactions, and aromaticity of substituted 1-(2-iminoethylidene) silan amine: a density functional study

The intramolecular hydrogen bond, molecular structure, π electrons delocalization, and vibrational frequencies in 1-(2-iminoethylidene) silan amine and its derivatives have been investigated by means of density functional method with 6-311++G** basis set, in gas phase, water, and carbon tetrachloride solutions. The obtained results showed that the hydrogen bond strength is mainly governed by resonance variations inside the chelate ring induced by the substituent groups. Furthermore, the topological properties of the electron density distributions for N–H···N intramolecular hydrogen bond were analyzed in terms of the Bader's theory of atoms in molecules. On the other hand, the aromaticity of the ring formed is measured using several well-established indices of aromaticity such as nucleus-independent chemical shift, harmonic oscillator models of the aromaticity, para-delocalization index, average two-center indices, aromatic fluctuation index, and π-fluctuation aromatic index. Natural population analysis data, the electron density and Laplacian properties, as well as γ(NH) and ν(NH) were further used for estimation of the hydrogen bonding interactions and the forces driving their formation.     

Studies on organotin compounds using the Del Re method : VII. Bond polarisability index and reactivity of organotin compounds

Using the Del Re method a simple reactivity index, defined as the bond polarisability index, has been derived. The observed reactivity sequence for the cleavage of the alkyl groups from the metalalkyls both in the polar and in the non-polar solvents have been interpreted, and the relative rates of these reactions correlated with this index. The relative rates of the exchange reactions between trialkylaluminium and trialkyltin hydrides have also been satisfactorily interpreted.