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31.
Both racemate and enantiomer of a novel double helix,binaphthylcyclooctaterthiophene(BN-COTh),which is a DNA-like molecule constructed by two single helices intertwined with each other via covalent bonds,have been synthesized with two building blocks,cycloocta-tetrathiophene(COTh) and cyclooctadinaphthyldithiophene(CONT) fused together via Negishi coupling reaction.Another homologue,dinaphthylcyclooctaterthiophene(DN-COTh) has been employed together as a model compound.Besides the synthetic work,BN-COTh and DN-COTh have been investigated by studying their crystal structures,spectroscopic behaviors,chiral resolution and chiral characteristics,including circular dichroism(CD) spectra and optical rotations.In addition,the novel crystal of enantiomer of(R,R,R)-BN-COTh has been explored.The enantiomer molecules packing along b-axis to form a larger and extended assembly packing due to intermolecular interactions between the enantiomer molecules and chloroform molecules in crystal. 相似文献
32.
Daniela Mazzier Soumen De Barbara Wicher Victor Maurizot Ivan Huc 《Angewandte Chemie (International ed. in English)》2020,59(4):1606-1610
A hydrogen‐bonding interface between helical aromatic oligoamide foldamers has been designed to promote the folding of a helix‐turn‐helix motif with a head‐to‐tail arrangement of two helices of opposite handedness. This design complements an earlier helix‐turn‐helix motif with a head‐to‐head arrangement of two helices of identical handedness interface. The two motifs were shown to have comparable stability and were combined in a unimolecular tetra‐helix fold constituting the largest abiotic tertiary structure to date. 相似文献
33.
In this article, we present the synthesis of a series of oligo(oxymethylenes) capped with 1‐phenylethanol and MeOH. The anionic condition affords enantiomerically pure oligo(oxymethylene) oligomers, while the cationic oligomerization leads to a racemic mixture of the oligo(oxymethylene) chain. 相似文献
34.
Artem V. Kabanov Vladislav M. Komarov 《International journal of quantum chemistry》2002,88(5):579-587
The origin of heterogeneity of nucleotide steps geometry in short double helixes is studied theoretically. By using the semiempirical MNDO/PM3 technique, the stability of “propeller‐like” and “step‐like” forms of base H‐pairing is examined in the structure of oligonucleotide duplexes of different types. The influence of end effects on the process of nucleotides packing, as well as the dependence of duplex curvature on the nature of bonded oligonucleotides, are examined. It is concluded that the structural polymorphism of base pairs most likely determines the unique packing of complementary pairs and their flexibility in DNA structure. © 2002 Wiley Periodicals, Inc. Int J Quantum Chem, 2002 相似文献
35.
Special crystallization event of isotactic polypropylene (iPP) in a constrained environment, a layered clay network, was followed by in situ Fourier transform infrared (FTIR) spectroscopy during the cooling process. Before occurrence of nucleation/crystallization, a conformationally ordered phase, which consists of significant amounts of long 31 helices with 14 monomeric units, has been identified for the first time. More importantly, it was found that the long‐ordering helices could play a more important role than short ones for the confined crystallization. It could be tentatively explained as due to the existence of constrained regions in the proximity of the nanoclay platelets or tactoids and the heterogeneous nucleation capability of the surface of nanoclay. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
36.
37.
在作者已给出的描述三螺旋蛋白质分子的哈密顿函数基础上,得到了孤立子存在的临界温度和热容器,其结果与实验结果一致。 相似文献
38.
Can Helical Peptides Unwind One Turn at a Time? ‐ Controlled Conformational Transitions in α,β2,3‐Hybrid Peptides 下载免费PDF全文
Dr. Dhayalan Balamurugan Dr. Kannoth M. Muraleedharan 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(26):9332-9338
Unfolding of helical trans‐β2,3‐hybrid peptides with (α–β)nα composition, when executed by increasing solvent polarity or temperature, proceeded in a systematic manner with the turns unwinding sequentially; C‐terminal region of these peptides were first to unwind and the process propagated towards N terminus with more and more β residues equilibrating from the gauche to the anti rotameric state across Cα?Cβ. This is evidenced by clear change in their CβH signal splitting, 3JCαH–CβH values, and sequential disappearance of i,i+2 NOEs. 相似文献
39.
《Macromolecular rapid communications》2017,38(15)
Conjugated polymers may be induced by intra‐ and/or intermolecular non‐covalent forces to fold into helical conformations. Helices formed by aromatic amide, hydrazide, and urea polymers possess a well‐organized cavity and depth, which is defined by their degree of polymerization. Driving forces may be intramolecular hydrogen bonding and/or solvophobicity, or guest induction. The resulting long helices represent a new class of unimacromolecular dynamic tubular architectures that exhibit unique properties or functions in, for example, molecular recognition, chirality transfer, and ion transporting. The recent advances are highlighted here.
40.
Koji YamamotoHiroki Sugiura Ryo AmemiyaHaruo Aikawa Zengjian AnMasahiko Yamaguchi Masashi Mizukami Kazue Kurihara 《Tetrahedron》2011,67(33):5972-5978
Optically active ethynylhelicene pentamers and hexamers linked by disulfide bonds were synthesized. They formed self-assembled monolayers (SAMs) with double helix structure on gold surfaces, which were analyzed by infrared reflection-absorption spectroscopy (IR-RAS), quartz crystal microbalance (QCM), surface plasmon resonance (SPR), and circular dichroism (CD). Double helix SAMs could be formed on gold surfaces either from double helices or random coils in solution. The double helices on the surface were more stable than in solution. This result suggested the presence of strong intercomplex interactions between double helix complexes on the surface. 相似文献