全文获取类型
收费全文 | 45篇 |
免费 | 1篇 |
专业分类
化学 | 29篇 |
晶体学 | 1篇 |
力学 | 5篇 |
数学 | 8篇 |
物理学 | 3篇 |
出版年
2023年 | 1篇 |
2021年 | 2篇 |
2020年 | 5篇 |
2019年 | 1篇 |
2017年 | 2篇 |
2016年 | 2篇 |
2015年 | 1篇 |
2014年 | 2篇 |
2013年 | 3篇 |
2012年 | 2篇 |
2011年 | 1篇 |
2010年 | 3篇 |
2009年 | 1篇 |
2008年 | 1篇 |
2004年 | 2篇 |
2003年 | 2篇 |
2002年 | 2篇 |
2001年 | 1篇 |
1999年 | 1篇 |
1998年 | 1篇 |
1994年 | 1篇 |
1984年 | 2篇 |
1981年 | 2篇 |
1974年 | 1篇 |
1972年 | 1篇 |
1970年 | 1篇 |
1968年 | 1篇 |
1966年 | 1篇 |
排序方式: 共有46条查询结果,搜索用时 31 毫秒
1.
We have studied the molecular dimensions of poly-2-vinylpyridine in solution in binary solvent mixtures consisting of a non polar and a polar component, viz. benzene-ethanol and benzene-chloroform. We have also studied the preferential solvation of the same polymer in the above mixtures using light scattering. We have observed a conformational transition of P2VP taking place in a composition region for each solvent mixture. This transition shows as a discontinuity in the unperturbed dimensions, in the long range interactions parameter and in the parameter of preferential solvation of the polymer. We think that this transition is related to the existence of two ordered structures of the polymer chain, one stable before and the other after the transition region. 相似文献
2.
3.
4.
Vasyl Hreb Vira Shved Oleh Buryy Olga Pekinchak Leonid Vasylechko 《无机化学与普通化学杂志》2020,646(14):1138-1143
Crystal structure parameters of the mixed cobaltite–chromite SmCo0.5Cr0.5O3 in the temperature range of 298–1173 K were derived from in situ high-resolution X-ray synchrotron powder diffraction data. Similar to the parent SmCoO3 compound, SmCo0.5Cr0.5O3 reveals anomalous thermal expansion reflected in abnormal temperature dependence of the unit cell dimensions and the selected interatomic distances and angles. These anomalies are associated with temperature induced changes of spin state of Co3+ ions and coupled insulator-metal transition. Observed decreasing behavior of the bandwidth W points on the increasing population of the exited spin states of Co3+ ions in SmCo0.5Cr0.5O3 with increasing temperature. First principle calculations revealed antiferromagnetic ground state of SmCo0.5Cr0.5O3 as the most stable. 相似文献
5.
Olha S. Panteleieva Vira V. Ponomarova Alexander V. Shtemenko Kostiantyn V. Domasevitch 《Acta Crystallographica. Section C, Structural Chemistry》2020,76(8):753-762
Anion…π interactions are newly recognized weak supramolecular forces which are relevant to many types of electron‐deficient aromatic substrates. Being less competitive with respect to conventional hydrogen bonding, anion…π interactions are only rarely considered as a crystal‐structure‐defining factor. Their significance dramatically increases for polyoxometalate (POM) species, which offer extended oxide surfaces for maintaining dense aromatic/inorganic stacks. The structures of tetrakis(caffeinium) μ12‐silicato‐tetracosa‐μ2‐oxido‐dodecaoxidododecatungsten trihydrate, (C8H11N4O2)4[SiW12O40]·3H2O, (1), and tris(theobrominium) μ12‐phosphato‐tetracosa‐μ2‐oxido‐dodecaoxidododecatungsten ethanol sesquisolvate, (C7H9N4O2)3[PW12O40]·1.5C2H5OH, (2), support the utility of anion…π interactions as a special kind of supramolecular synthon controlling the structures of ionic lattices. Both caffeinium [(HCaf)+ in (1)] and theobrominium cations [(HTbr)+ in (2)] reveal double stacking patterns at both axial sides of the aromatic frameworks, leading to the generation of anion…π…anion bridges. The latter provide the rare face‐to‐face linkage of the anions. In (1), every square face of the metal–oxide cuboctahedra accepts the interaction and the above bridges yield flat square nets, i.e. {(HCaf+)2[SiW12O40]4?}n. Two additional cations afford single stacks only and they terminate the connectivity. Salt (2) retains a two‐dimensional (2D) motif of square nets, with anion…π…anion bridges involving two of the three (HTbr)+ cations. The remaining cations complete a fivefold anion…π environment of [PW12O40]3?, acting as terminal groups. This single anion…π interaction is influenced by the specific pairing of (HTbr)+ cations by double amide‐to‐amide hydrogen bonding. Nevertheless, invariable 2D patterns in (1) and (2) suggest the dominant role of anion…π interactions as the structure‐governing factor, which is applicable to the construction of noncovalent linkages involving Keggin‐type oxometalates. 相似文献
6.
Ponomarova VV Komarchuk VV Boldog I Chernega AN Sieler J Domasevitch KV 《Chemical communications (Cambridge, England)》2002,(5):436-437
Cross-linking of corrugated square grid coordination layers by anionic bridging groups generates five-connected coordination networks; the 3D topologies of mixed-anion cobalt(II) and nickel(II) complexes with a tetramethyl-substituted 4,4'-bipyrazolyl ligand are supported by mu-SO4(2-) functions and exist as neutral or cationic five-connected arrays involving additional terminal (NCS-) or non-coordinated (NO3-, ClO4-) groups. 相似文献
7.
M. A. Sinel’nikova E. N. Shved V. V. Usachev N. M. Oleinik 《Theoretical and Experimental Chemistry》2010,46(3):168-175
A model was constructed for the mechanism of the reaction of aliphatic and aromatic carboxylic acids with epichlorohydrin
catalyzed by tertiary amines. A mechanism for the catalysis of the transfer of the anion of the nucleophilic reagent by an
ion pair was proposed taking account of the kinetic data and selected chemical and mathematical models. 相似文献
8.
9.
Tamara Bezrodna Georgyi Klishevich Volodymyr Melnyk Vira Nesprava Olexandr Roshchin 《Molecular Crystals and Liquid Crystals》2020,697(1):60-67
AbstractFluorescence and absorption spectra of the 2-fluoronaphthalene admixtures in naphthalene were studied at low temperature (T?=?4.2 К). Two types of pairwise impurity centers were formed at admixture concentrations of more than 1?wt%. Polarization of absorption bands was detected; these spectra were determined by resonance interactions between molecules of the impurity center. Resonant splitting of electronic levels for the translationally nonequivalent molecules in the unit cell of the naphthalene crystal was analyzed for the case, when one molecule was in the similar phase with the incident light wave and the other one was in antiphase. 相似文献
10.
Vira V. Ponomarova Konstantin V. Domasevitch 《Acta Crystallographica. Section C, Structural Chemistry》2012,68(9):o359-o361
In the title compound, 2C9H6N2O2·C12H24O6·4H2O, the 18‐crown‐6 (1,4,7,10,13,16‐hexaoxacyclooctadecane) molecule resides across a centre of inversion. The adduct exists as a molecular hydrogen‐bonded complex featuring integration of two kinds of synthons, viz. [(18‐crown‐6)(H2O)4] [O...O = 2.8645 (18)–2.9014 (18) Å] and an oxime/aqua ensemble, PhC(O)C(CN)NOH...OH2 [O...O = 2.5930 (18) Å]. The reliability of the oxime/aqua motif, sustained by the highly acidic cyanooxime, is an essential factor in the construction of multicomponent cocrystals and the accommodation of oxime species in macrocyclic hosts. The supramolecular structure is generated by the alternation of hydrophilic [(18‐crown‐6)(H2O)4] layers and bilayers of benzoyl(hydroxyimino)acetonitrile molecules, resulting in stacking interactions between the phenyl and cyano groups of 3.666 (2) Å. 相似文献