6, 6-Dialkyl- und 6, 6-Polymethylen-fulvene

The electronic, infrared and NMR spectra of 6, 6-dialkyl-fulvenes and of 6, 6-poly-methylene-fulvenes are reported.     

6A6B, 6A6C,and 6A6D-ditosylates of β-cyclodextrin

Regio-isomers, 6A6B, 6A6C, and 6A6D-ditosylates of β-cyclodextrin prepared by the reaction of β-cyclodextrin with tosyl chloride were easily and effectively separated through reversed phase column chromatography and assigned.     

Preparation of 6-chloro-6-desoxy- and 6-iodo-6-desoxycellulose

Conclusions The reaction of 2,3-di-O-acetylcellulose with N-chloro- or N-iodosuccinimide and triphenylphosphine gave the 6-chloro-6-desoxy- and 6-iodo-6-desoxycellulose acetates with a respective degree of substitution (DS) in halogen of 0.8–1.0 and 0.7. The deacetylation of these compounds gave 6-chloro-6-desoxycellulose (DS 0.8) and 6-iodo-6-desoxycellulose (DS 0.6).Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2158–2160, September, 1977.     

Isomer stability of N6C6H6 cages

Recent theoretical studies have identified carbon-nitrogen cages that are potentially stable high energy density materials (HEDM). One such molecule is an N(6)C(6)H(6) cage in which a six-membered ring of nitrogen is bonded to C(3)H(3) triangles on both sides. This molecule is based on the structure of the most stable N(12) cage, with six carbon atoms substituted into the structure. In the current study, several N(6)C(6)H(6) isomers (including the previously studied cage) are examined by theoretical calculations to determine which is actually the most stable. Stability will be evaluated from two points of view: (1) thermodynamic stability of one isomer versus another and (2) kinetic stability of each isomer as determined by the energetics of bond breaking. Density functional theory (B3LYP), perturbation theory (MP2 and MP4), and coupled-cluster theory (CCSD(T)) are used in this study, along with the correlation-consistent basis sets of Dunning. Trends in thermodynamic and kinetic stability are discussed.     

Regioselective synthesis of 6-amino- and 6-amido-6-deoxypullulans

Hydrophobically modified polysaccharides that contain amine and amide groups possess valuable features for drug delivery and other applications. These chemical groups are known to play a fundamental role in the biological activity of important polysaccharides. Pullulan is known for its non-toxicity and biocompatibility, therefore, we have applied the versatile Staudinger reaction for the synthesis of regioselectively substituted pullulan derivatives containing amine or amide groups with promise for biomedical applications. The synthesis began with the regioselective bromination of pullulan at C-6 with N-bromosuccinimide and triphenylphosphine, providing 6-bromo-6-deoxy-pullulan, which is soluble in a range of organic solvents and therefore is a dynamic intermediate for the synthesis of other pullulan derivatives. Azide displacement of bromide from 6-bromo-6-deoxy-pullulan esters yielded the corresponding 6-azido-6-deoxy-pullulan esters. Staudinger reduction of these azides efficiently and chemoselectively afforded the corresponding amino- or amidopullulans.     

Electron scattering on C6F6 and SF6 molecules

Total absolute cross sections for electron scattering on hexafluorobenzene, C₆F₆, and sulfur hexafluoride, SF₆, molecules, have been measured as a function of impact energy from 0.6 to 250 eV. The total cross section for C₆F₆ exhibits a very broad peak stretching from 10 to 100 eV with some weak features near 9.5 and 15 eV superimposed on the peak. Apart from the well-known low-energy resonant structures in the SF6 total cross section function, a new weak resonant feature close to 25 eV has been noticed in the present experiment, in accordance with earlier theoretical calculations.     

Discrete copper(I) clusters with Cu6P6Se6 and Cu6P4Se6 cores

The reactions of chalcogenophosphinites with copper(I) metal salts are shown to yield highly stable, multi-metallic copper-chalcogen based clusters with novel topologies.     

金属原子（离子）-苯配合物的电子转移反应

用密度泛函理论（ＤＦＴ／ＢＬＹＰ）在６－３１Ｇ基组水平上研究了金属原子－苯与离子－苯配合物的气相电子转移过程,得到了Ｍ（Ｌｉ,Ｎａ,Ｍｇ）－Ｃ６Ｈ６和Ｍ＾＋－Ｃ６Ｈ６络合物以及它们之间电子转移过程的先驱络合物的最优几何构型和电子结构。同时,利用线性坐标确定了过滤态的结构,结果表明：ＤＦＴ方法计算得到的单体,即原子（离子）－苯的构型,同ＭＰ２结果较为一致。先驱络合物具有Ｃ６ν对称性,给体与受体间距离     

Theoretical study of migrational nonrigidity of molecules of salts of closo-boranes Li2B6H6, BeB6H6, (BeH)2B6H6, and LiB6H6 −

Institute for New Chemical Problems, Academy of Sciences of the USSR. Translated from Zhurnal Strukturnoi Khimii, Vol. 30, No. 2, pp. 7–18, March–April, 1989.     

Regioselective synthesis of 6-alkyl- and 6-prenylpolyhydroxyisoflavones and 6-alkylcoumaronochromone derivatives

The palladium-catalyzed coupling reaction of 6-iodoisoflavone, prepared from 3'-iodoacetophenone derivative, with 2-methyl-3-butyn-2-ol gave 6-alkynylisoflavone derivative, which was hydrogenated to give 6-alkylhydroxyisoflavone (luteone hydrate) (2). Dehydration of 2 gave 2',4',5,7-tetrahydroxy-6-prenylisoflavone (luteone) (1). Wighteone hydrate (3) was also synthesized from 6-iodotris(benzyloxy)isoflavone in a similar manner. 6-Alkyl-4'5,7-trihydroxy-coumaronochromone (4) was synthesized by oxidative cyclization of 2 with o-chloranil.     

Application of algebraic method to the high overtones of C6H6 and C6D6

Both the spectra and infrared transition strengths of C₆H₆ and C₆D₆ for the C? H stretching overtones up to as high as v = 10 are described in high precision with few parameters (six for the spectra and four for the transition strengths) by the Iachello–Oss algebraic model. The Hamiltonian model is solved in the symmetry adapted bases, which are constructed by the symmetrized boson representation (SBR) technique. The results show that the combination of the algebraic method and SBR technique is a powerful method for describing vibrations of large molecules and high overtones. © 2004 Wiley Periodicals, Inc. Int J Quantum Chem, 2005