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31.
Synthesis and X-ray structural study of octa-coordinated hexafluoroacetylacetone hafnium(IV) complex
K. V. Zherikova N. B. Morozova I. A. Baidina V. I. Alekseev I. K. Igumenov 《Journal of Structural Chemistry》2006,47(1):82-86
Hexafluoroacetylacetonate hafnium(IV) complex has been synthesized and studied by X-ray structural analysis. Crystal data for C30H8F36Hf2O14 are: a = 12.957(3) Å, b = 16.687(3) Å, c = 12.398(3) Å, β = 108.97°, space group P21/c, Z = 2, d calc = 2.137 g/cm3, R = 0.047. The molecular structure is built from discrete binuclear molecules of Hf2(OH)2(hfac)6 composition; the Hf...Hf distance in dimer is 3.533 Å. The structural units are connected by van der Waals interactions in the crystal. 相似文献
32.
N. B. Morozova A. E. Turgambaeva I. A. Baidina V. V. Krysyuk I. K. Igumenov 《Journal of Structural Chemistry》2005,46(6):1047-1051
The structure of titanyl dipivalylmethanate TiO(dpm)2 has been studied by X-ray diffraction analysis. The compound has a molecular structure formed by isolated centrosymmetrical dimers [TiO(dpm)2]2; the unit cell contains two structurally related, crystallographically unique binuclear molecules. The Ti...Ti distance in the dimer is 2.73 Å. Crystal data for Ti2C36H76O10: a = 32.477(6) Å, b = 14.409(3) Å, c = 25.630(5) Å; β = 107.82(3)°, space group C2/c, Z = 8, d calc = 1.002 g/cm3. 相似文献
33.
Ziya Kantarci Celal Bayrak 《Journal of inclusion phenomena and macrocyclic chemistry》1998,30(1):59-68
IR spectra of Mn(trimethylenediamine)Zn(CN)42C6H6 and IR and Raman spectra of Zn(trimethylenediamine)Zn(CN)4_2C6H6 are reported. The spectral data suggest that the host frameworks of these compounds are similar to those of the tn-Td-type Cd(trimethylenediamine)M(CN)4_2benzene (M = Cd or Hg) and the chelated pn-Td-type Cd(propylenediamine)Cd(CN)4_1,2-dichloro-ethane clathrates, respectively. 相似文献
34.
E. V. Kalashnikova K. D. Shcherbakova E. Smolková-Keulemansová L. Feltl 《Chromatographia》1992,33(1-2):10-12
Summary A study has been made of the interaction between graphitized thermal carbon-black and cyclodextrins and a series of 28 derivatives of benzene (benzene, alkyl-, isoalkyl-, dialkyl-, trialkylbenzenes, vinyl-, and allyl-benzene). The specificretention volumes form the basis for a discussion of the mechanism of interaction and drawing conclusions for the practical separation of isomeric compounds. 相似文献
35.
36.
A. N. Ageev A. A. Aratskova L. D. Belyakova T. N. Gvozdovich A. V. Kiselev Ya. I. Yashin J. Kàlal F. Švec 《Chromatographia》1983,17(10):545-548
Summary The retention of benzene derivatives with nonpolar and polar substituents on a porous methacrylate copolymer containing epoxy groups using both nonpolar and polar eluents was investigated. When n-hexane is used as the eluent, the retention of n-alkylbenzenes and polymethylbenzenes is weaker than that of benzene. In the case of benzene derivatives containing polar functional groups their capacity ratios (k) on this porous polymer increases approximately linearly with the increase of the adsorbate molecules dipole moment. The retention characteristics of the methacrylate copolymer were compared with that of a styrene-divinylbenzene copolymer and silica gels with a hydroxylated surface and with a surface modified by chemically bonded alkylsilyl groups. 相似文献
37.
The synthesis of dendrons with the end-capped 5-(N,N-dimethylamino)naphthyl-1-ethynyl unit connected to conjugated naphthylethynyl or p-phenylethynyl chains, as the branches of the 1,3,5-substituted benzene core, have been undertaken by heterocoupling reaction between 1,3,5-triiodobenzene and the convenient end-capped 5-(N,N-dimethylamino)naphthylacetylene or 5-(N,N-dimethylamino)naphthylethynylphenylacetylene in the presence of the palladium-copper catalyst system, in excellent yields. The influence of the alternating naphthylethynyl-phenylethynyl chains on the fluorescence emission radiation, in the dendron structures, has been analyzed. 相似文献
38.
Schultz György Hargittai István Rot Nicolette Bickelhaupt Friedrich 《Structural chemistry》1998,9(3):209-214
The molecular structure of 1,3,5-tris (trimethylstannyl) benzene has been determined by gas-phase electron diffraction. The C — C bond length is in good agreement with that in benzene. In agreement with the somewhat electron-releasing character of the substituents, the endocyclic bond angles at the substituents are somewhat smaller than 120°. The mean value of Sn — C bond lengths is greater than that in tetraphenyltin and tetramethyltin. The SnMe3 groups appear freely rotating around the Caryl — Sn bonds. The following bond lengths (r
g) and bond angles were determined: (Sn — C)mean 2.150 ± 0.007 Å, C — C 1.399 ± 0.005 Å, (C — H)mean 1.105 ± 0.006 Å, < C — C(Sn) — C 117.7 ± 1.7º, < Caryl — Sn — Cmethyl 106.7 ± 0.7º < Sn — C — H 111.5 ± 0.9º. 相似文献
39.
Ti接枝MCM-41催化剂的结构设计及化学亲和选择性研究 总被引:3,自引:0,他引:3
用二氯化钛茂作为活性物种的来源,利用Si-MCM-41催化剂表面羟基的反应性,得到了Ti接枝MCM-41催化剂的两种结构模型.结构表征结果表明,Ti接枝MCM-41催化剂不仅长程结构好,孔径分布均一,而且催化剂表面活性中心含量高.两种结构模型催化剂上芳烃羟化反应性能表明,Ti接枝MCM-41催化剂表面的亲水/憎水性可以在较宽的范围内调变,从而可实现控制芳烃羟化的化学亲和选择性.另外,研究结果还表明,Ti接枝MCM-41催化剂具有很好的活性稳定性. 相似文献
40.
Constantinos D. Diakoumakos John A. Mikroyannidis Christoforos A. Krontiras Michael N. Pisanias 《Journal of polymer science. Part A, Polymer chemistry》1994,32(10):1915-1921
New thermosetting resins were prepared from the reaction of 1,4-bis(2,2-dicyanovinyl)benzene with aromatic diamines in varying molar ratios. The thermal stability of these resins was correlated with their composition and the curing conditions. They were stable in N2 up to 370–448°C and afforded anaerobic char yields of 73–84% at 800°C after curing at 300°C for 20–60 h. The temperature dependence of the electrical resistivity of all resins pyrolyzed at 700°C for 15 h was studied in the temperature range from ?173–327°C (100–600 K). The results showed that at room temperature the unpyrolyzed polymers have insulating properties, whereas a dramatic decrease in the electrical resistivity is observed following pyrolysis. The temperature dependence of the electrical resistivity suggests that all of the materials studied have semiconducting properties. The observed electrical conductivity is thermally activated with activation energies ranging from 0.03–0.06 eV. © 1994 John Wiley & Sons, Inc. 相似文献