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1.
2.
D. N. Dybtsev M. P. Yutkin E. V. Peresypkina A. V. Virovets Y. Hasegawa H. Nishihara V. P. Fedin 《Russian Chemical Bulletin》2007,56(9):1782-1786
The reaction of Co(NO3)2·6H2O with 1,3,5-benzenetricarboxylic acid (H3btc, trimesic acid) in DMF at 100 °C afforded the coordination polymer [Co3(dmf)6(btc)(Hbtc)(H2btc)]··9H2O (1) (dmf is N,N′-dimethylformamide, DMF). According to the X-ray diffraction study, the metal-organic coordination polymer is composed of
planar honeycomb (6,3) networks, in which the organic benzenetricarboxylate anions and the inorganic Co2+ cations play a role of three-connected nodes. Disordered water molecules are intercalated between the layers. A study of
the magnetic properties showed the presence of a weak antiferromagnetic coupling between the Co2+ ions (S = 3/2).
Dedicated to Academician G. A. Abakumov on the occasion of his 70th birthday.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1719–1723, September, 2007. 相似文献
3.
N. K. Eremenko S. S. Kurasov A. V. Virovets T. Struchkov V. V. Bashilov V. I. Sokolov 《Russian Chemical Bulletin》1997,46(1):164-167
New platinum-mercury clusters, Pt4(HgX)2(μ-CO)4(PR3)4 (X=Cl, Br, I, CF3, or CCl3; R=Ph or Et), were synthesized. The molecular and crystal structure of the Pt4(HgBr)2(μ-CO)4(PPh3)4 cluster was established by X-ray structural analysis. 相似文献
4.
Crystal structure of di (1-n-dodecylpyridine) decahydro-closo-decaborate(2-) (C5H5N-C12H25)2[B10H10]
A. V. Virovets N. N. Vakulenko V. V. Volkov N. V. Podberezskaya 《Journal of Structural Chemistry》1994,35(3):339-344
Using X-ray analysis, we have determined the crystal structure of di(1-n-dodecylpyridine) decahydrocloso-decaborate(2-), (py-C12H25)2[B10H10] (I), a yellow salt-like substance obtained by reaction of (py-C12H25)Br and K2[B10H10] in an aqueous solution. Compound I melts at 1250 without decomposition and luminesces under ultraviolet radiation (λmax=555 nm at 298 K). In I, quaternary pyridine bases, containing a hydrocarbon radical with the C12 chain, are combined with the closo-cluster hydroborate anion [B10H10]2-. This results in a charge transfer structure having shortened nonvalent (equatorial B) H.…H(C of pyridine) contacts of 2.41(8) Å. Crystals I are orthorhombic with a=8.584 (1), b=7.739(1), c=31.183(5) Å, Vcell=2071.4(5) Å3, space group Pnmm, Z=2, dcalc=0.986 g/cm3 (a Syntex P21 automatic diffractometer, λCUKα, Nmsd/used=1654/711, Raniso=0.076, Rw=0.080, w=1/(σ(Fobs)2+0.0007·F obs 2 ). Substantial changes are observed in the vibration range of the valent B?H bonds in the IR spectrum of I as compared to that of pure ionic K2[B10H10], confirming the interaction. 相似文献
5.
A. V. Virovets N. V. Podberezskaya M. N. Sokolov I. V. Korobkov V. P. Fedin V. E. Fedorov 《Journal of Structural Chemistry》1993,34(2):292-295
The crystal structure was determined for Nb2S4(S2NCEt2)4 obtained in 48% yield by the reaction of Cs4Nb2S4(NCS)8 with NaS2CNEt2 in water: a=21.181(8), b=6.958(1), c=16.623(6) Å, =133.95(2)o, V = 1764(1) Å3, space group C2/m, Z=2, dcalc=1.708 g/cm3. The measurements were carried out on a Syntex P21 diffractometer with CuK radiation. A total of 2536 reflections were measured, of which 990 were used, Raniso=0.0444. The basic fragment in this molecule is [Nb2(2–S2)2]4+, the Nb–Nb distance in which corresponds to a metal-metal single bond. The molecule is partially disordered over two positions about the twofold axis and mirror plane of the C2/m space group. The dithiocarbamate and disulfide ligands with bidentate coordination form a distorted square antiprism about each of the niobium atoms as in NbS2Cl2. The anomalously large S–S bond length in the S2 ligand [2.282(5) Å] may be attributed to inaccuracy in the determination due to disorder.Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated from Zhurnal Strukturnoi Khimii, Vol. 34, No. 2, pp. 134–138, March–April, 1993. 相似文献
6.
Synthesis and Crystal Structure of Supramolecular Adducts of Macrocyclic Cavitand Cucurbituril with Chromium(III) and Nickel(II) Aqua Complexes 总被引:1,自引:0,他引:1
Samsonenko D. G. Geras'ko O. A. Mit'kina T. V. Lipkowski J. Virovets A. V. Fenske D. Fedin V. P. 《Russian Journal of Coordination Chemistry》2003,29(3):166-174
Supramolecular compounds {[Cr(H2O)6](C36H36N24O12)}(NO3)3 · 13H2O (I) and {[Ni(H2O)6]2(C36H36N24O12)}(SO4)2 · 16H2O (II) were obtained from aqueous solutions of chromium nitrate or nickel sulfate and the macrocyclic cavitand cucurbituril. According to X-ray diffraction analysis data, the cucurbituril molecule is closed from both sides by metal aqua complexes due to the formation of hydrogen bonding between the cucurbituril CO groups and aqua ligands. Compound I has a chain structure, while the structure of compound II is layered. Modes of cucurbituril coordination, depending on the size and charge of the metal cation, are discussed. 相似文献
7.
A. V. Virovets S. N. Konchenko P. S. Yuferov D. Fenske 《Journal of Structural Chemistry》2004,45(3):496-501
The crystal structures of three cluster compounds: [(µ-H)Fe2Mo(µ3-Te)(CO)8Cp*], [FeMo2(µ3-Te)(CO)7x Cp*2], and [FeMoW(µ3-Te)(CO)7CpCp*], where Cp = 5-C5H5, Cp* = 5-C5 (CH3)5, have been investigated. In the cluster with a tetrahedral {FeMo2Te} core, one can observe positional isomerism of the carbonyl and cyclopentadienyl ligands with respect to the plane through the Fe and Te atoms and the center of the Mo2bond, resulting in two mirror isomers in the racemic crystal. In the cluster with the {FeMoWTe} core, additional chirality causes the formation of four diastereoisomers. Earlier, the structure of the [FeMoW(µ3-Se)(CO)7Cp] cluster with Mo and W atoms coordinated to identical Cp-ligands has been structurally defined. In this crystal, statistical disordering of Mo and W over the metal positions is observed. In the [FeMo(Cp*)W(Cp)(µ3-Te)(CO)7] cluster studied here, the Mo and W atoms are coordinated to different cyclopentadienyl ligands. Due to this, two of four diastereoisomers were isolated as ordered racemic crystals; the other two are nonexistent for steric reasons.Original Russian Text Copyright © 2004 by A. V. Virovets, S. N. Konchenko, P. S. Yuferov, and D. FenskeTranslated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 3, pp. 522–527, May–June 2004. 相似文献
8.
Sokolov MN Gushchin AL Virovets AV Peresypkina EV Kozlova SG Fedin VP 《Inorganic chemistry》2004,43(25):7966-7968
Black single crystals of Ta(4)Se(9)I(8) are obtained in a high yield by heating Ta, Se, and I(2) at 300 degrees C in 1:2.2:1.0 molar ratio. In the structure, the tantalum atoms form a square, with four Se(2) ligands bridging the Ta-Ta edges and one capping the square. Each Ta atom has two terminal iodine atoms. The compound is diamagnetic and has only two electrons for metal-metal bonding. 相似文献
9.
Alexander V. Virovets Sergey N. Konchenko 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(9):e383-e384
The structure of the title compound, hexacarbonyl‐1κ3C,2κ3C‐[3(η5)‐cyclopentadienyl]bis(μ3‐selenido)diiron(II)cobalt(II),[CoFe2(μ3‐Se)2(C5H5)(CO)6], was redetermined at room temperature and the correct C2/c space group was assumed instead of the previously reported P space group [Mathur et al. (1995). Organometallics, 14 , 2115–2118]. Analysis of the literature data showed that the previously reported triclinic parameters correspond to a primitive subcell of the actual monoclinic C‐centred cell with cell dimensions close to those found by us. The title compound appeared to be isostructural with the sulfur–selenium analogue. 相似文献
10.
Naumov N. G. Artemkina S. B. Virovets A. V. Fedorov V. E. 《Russian Journal of Coordination Chemistry》2004,30(11):792-799
The [{Mn(H2O)3}2{Re6Se8(CN)6}] · 3.3H2O complex was produced on slow evaporation of an aqueous solution containing the salt of a cluster complex K4Re6Se8(CN)6 · 3.5H2O and a 23-fold excess of Mn2+. The cluster complexes [Re6Se8(CN)6]4– are linked in a crystal into the charged coordination layers [{Mn(H2O)3}4{Re6Se8(CN)6}3]4–
2 through the Mn2+ cations. The Mn2+ cations are coordinated in a layer by three cyano nitrogen atoms of the cluster complexes; the Mn–N bond lengths are 2.13(4) and 2.21(2) Å. Each [Re6Se8(CN)6]4– anion is bonded to three manganese cations Mn(1). The anions are bonded additionally to the Mn(2) cations disordered over two close positions. 相似文献