全文获取类型
收费全文 | 394篇 |
免费 | 12篇 |
国内免费 | 2篇 |
专业分类
化学 | 332篇 |
晶体学 | 2篇 |
力学 | 2篇 |
数学 | 10篇 |
物理学 | 62篇 |
出版年
2022年 | 2篇 |
2021年 | 1篇 |
2020年 | 7篇 |
2019年 | 3篇 |
2018年 | 1篇 |
2016年 | 4篇 |
2015年 | 4篇 |
2014年 | 16篇 |
2013年 | 34篇 |
2012年 | 26篇 |
2011年 | 36篇 |
2010年 | 12篇 |
2009年 | 11篇 |
2008年 | 20篇 |
2007年 | 30篇 |
2006年 | 20篇 |
2005年 | 23篇 |
2004年 | 19篇 |
2003年 | 14篇 |
2002年 | 12篇 |
2001年 | 11篇 |
2000年 | 11篇 |
1999年 | 4篇 |
1998年 | 2篇 |
1997年 | 1篇 |
1996年 | 1篇 |
1995年 | 5篇 |
1994年 | 4篇 |
1993年 | 4篇 |
1992年 | 6篇 |
1991年 | 9篇 |
1990年 | 7篇 |
1989年 | 3篇 |
1988年 | 6篇 |
1987年 | 3篇 |
1986年 | 1篇 |
1985年 | 2篇 |
1984年 | 3篇 |
1982年 | 5篇 |
1981年 | 1篇 |
1980年 | 1篇 |
1979年 | 2篇 |
1978年 | 6篇 |
1977年 | 4篇 |
1976年 | 1篇 |
1974年 | 3篇 |
1973年 | 2篇 |
1970年 | 1篇 |
1969年 | 2篇 |
1968年 | 1篇 |
排序方式: 共有408条查询结果,搜索用时 31 毫秒
1.
Ichiro Hisaki Shoichi Nakagawa Norimitsu Tohnai Mikiji Miyata 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2015,127(10):3051-3055
A C3‐symmetric π‐conjugated macrocycle combined with an appropriate hydrogen bonding module (phenylene triangle) allowed the construction of crystalline supramolecular frameworks with a cavity volume of up to 58 %. The frameworks were obtained through non‐interpenetrated stacking of a hexagonal sheet possessing three kinds of pores with different sizes and shapes. The activated porous material absorbed CO2 up to 96 cm3 g−1 at 195 K under 1 atm. 相似文献
2.
3.
4.
5.
Takahiro Miyata Kozo Matsumoto Takeshi Endo Shigeaki Yonemori Shoji Watanabe 《Journal of polymer science. Part A, Polymer chemistry》2012,50(15):3046-3051
A styrene‐based monomer having a five‐membered cyclic carbonate structure, 4‐vinylbenzyl 2,5‐dioxoran‐3‐ylmethyl ether (VBCE), was prepared by lithium bromide‐catalyzed addition of carbon dioxide to 4‐vinylbenxyl glycidyl ether (VBGE). Radical polymerization of the obtained VBCE was carried out using 2,2′‐azobisisobutyronitrile as an initiator. PolyVBCE with number‐averaged molecular weight higher than 13,800 was obtained by a solution polymerization in N,N‐dimethylformamide, N,N‐dimethylacetamide, dimethyl sulfoxide, and methyl ethyl ketone. The glass transition temperature and 5 wt % decomposition temperature of the polyVBCE were determined to be 52 and 305 °C by differential scanning calorimetry and thermal gravimetry analysis, respectively. It was confirmed that a polymer consisting of the same VBCE repeating unit can be also obtained via chemical modification of polyVBGE, that is, a lithium‐bromide‐catalyzed addition of carbon dioxide to a polyVBGE prepared from a radical polymerization of VBGE. Further copolymerization of VBCE with styrene gave the corresponding copolymer in a high yield. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
6.
Misa Sugino Keisuke Hatanaka Tetsuya Miyano Ichiro Hisaki Mikiji Miyata Aya Sakon Hidehiro Uekusa Norimitsu Tohnai 《Tetrahedron letters》2014
An organic salt composed 9,10-bis(4-aminophenyl)anthracene and hypophosphorous acid emits yellow-green fluorescence in the crystalline state. The salt also gives water inclusion crystal which provides blue-green fluorescence. Single X-ray crystal studies revealed that water molecules induced the fluorescence change resulting from reaggregation of molecular packing. 相似文献
7.
Yusuke Shiraki Kazuhiro Tsuruta Junpei Morimoto Chihiro Ohba Akifumi Kawamura Ryo Yoshida Ryuji Kawano Tadashi Uragami Takashi Miyata 《Macromolecular rapid communications》2015,36(6):515-519
Microdevices designed for practical environmental pollution monitoring need to detect specific pollutants such as dioxins. Bisphenol A (BPA) has been widely used as a monomer for the synthesis of polycarbonate and epoxy resins. However, the recent discovery of its high potential ability to disrupt human endocrine systems has made the development of smart systems and microdevices for its detection and removal necessary. Molecule‐responsive microsized hydrogels with β‐cycrodextrin (β‐CD) as ligands are prepared by photopolymerization using a fluorescence microscope. The molecule‐responsive micro‐hydrogels show ultra‐quick shrinkage in response to target BPA. Furthermore, the flow rate of a microchannel is autonomously regulated by the molecule‐responsive shrinking of their hydrogels as smart microvalves.
8.
Kotaro Hayashi Hiroyuki Chaya Shigeto Fukushima Sumiyo Watanabe Hiroyasu Takemoto Kensuke Osada Nobuhiro Nishiyama Kanjiro Miyata Kazunori Kataoka 《Macromolecular rapid communications》2016,37(6):486-493
Polyion complexes (b‐PICs) are prepared by mixing single‐ or double‐stranded oligo RNA (aniomer) with poly(ethylene glycol)‐b‐poly(l ‐lysine) (PEG‐PLL) (block catiomer) to clarify the effect of aniomer chain rigidity on association behaviors at varying concentrations. Here, a 21‐mer single‐stranded RNA (ssRNA) (persistence length: 1.0 nm) and a 21‐mer double‐stranded RNA (small interfering RNA, siRNA) (persistence length: 62 nm) are compared. Both oligo RNAs form a minimal charge‐neutralized ionomer pair with a single PEG‐PLL chain, termed unit b‐PIC (uPIC), at low concentrations (<≈0.01 mg mL−1). Above the critical association concentration (≈0.01 mg mL−1), ssRNA b‐PICs form secondary associates, PIC micelles, with sizes up to 30–70 nm, while no such multimolecular assembly is observed for siRNA b‐PICs. The entropy gain associated with the formation of a segregated PIC phase in the multimolecular PIC micelles may not be large enough for rigid siRNA strands to compensate with appreciably high steric repulsion derived from PEG chains. Chain rigidity appears to be a critical parameter in polyion complex association.
9.
Back Cover: Amphiphilic Inclusion Spaces for Various Guests and Regulation of Fluorescence Intensity of 1,8‐Bis(4‐aminophenyl)anthracene Crystals (Chem. Eur. J. 11/2014) 下载免费PDF全文
10.
We report the generation of a nano-scale tubular structure of cellulose molecules (CelNT), through density functional theory (DFT) calculations. When a cellulose IIII (1 0 0) chain sheet model is optimized by DFT calculations, the sheet models spontaneously roll into tubes. The oligomers arrange in a right-handed, four-fold helix with one-quarter chain staggering, oriented with parallel polarity similar to the original crystal structure. Based on a one-quarter chain staggering relationship, six large CelNT models, consisting of 16 cellulose chains with DP = 80, are constructed by combinations of two types of chain polarities and three types of symmetry operations to generate a circular arrangement of molecular chains. All six CelNT models are examined by molecular dynamics (MD) calculations in chloroform. While four CelNT models retain a tubular form throughout MD calculations, the remaining two deform. 3D-RISM theory model is used to estimate the solvation free energies of the four CelNT models. The results suggest that the CelNT model with a chain arrangement of parallel polarity and right-handed helical symmetry forms the most stable tube structure. 相似文献