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661.
H. Yasuda H. Mori T. Muraki T. Sakata 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1994,29(3):209-212
The negative ion photoelectron spectrum of7Li
2
–
is reported at 488 nm (2.540 eV). Three electronic bands are observed in this spectrum and are assigned to the following photodetachment transitions:7Li2,X
1
g
+
+e
– 7Li
2
–
,X
2
u
+
;7Li2,a
3
u
+
+e
– 7Li
2
–
,X
2
u
+
; and7Li2,A
1
u
+
+e
– 7Li
2
–
,X
2
u
+
. The electron affinity of7Li2 is determined to be 0.437±0.009 eV, leading to an anion dissociation energy,D
0, of 0.865±0.022 eV for the ground state of7Li
2
–
. A Franck-Condon analysis of the7Li2,X
1
g
+
+e
– 7Li
2
–
,X
2
u
+
band yields the following spectroscopic constants for the ground state of7Li
2
–
:B
e
=0.502±0.005 cm–1,r
e
=3.094±0.015 Å, and
e
=232±35 cm–1. 相似文献
662.
Nobuhiro Yasuda Hidehiro Uekusa Yuji Ohashi 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(11):1364-1366
The crystal structures of two styrene analogues, 4‐vinylbenzoic acid, C9H8O2, (I), and 9‐vinylanthracene, C16H12, (II), were determined by X‐ray analyses at 108 and 293 K for (I) and at 123 and 293 K for (II). In (I), a pair of molecules around an inversion center form a dimer connected by two carboxyl groups. The anthracene planes of two molecules in (II) are antiparallel to each other around an inversion center. The vinyl group of (I) is almost coplanar with the phenyl ring, whereas the vinyl group of (II) is nearly perpendicular to the anthracene plane. In (I), the bond length of the vinyl group at 293 K is significantly shorter than that at 108 K [1.288 (2) versus 1.3248 (14) Å] suggesting a bias of the thermal motion, whereas the bond lengths are not so different between the two temperatures in (II) [1.3266 (15) versus 1.310 (2) Å]. 相似文献
663.
664.
Copper‐Catalyzed Enantioselective Allyl–Allyl Coupling between Allylic Boronates and Phosphates with a Phenol/N‐Heterocyclic Carbene Chiral Ligand 下载免费PDF全文
Yuto Yasuda Prof. Dr. Hirohisa Ohmiya Prof. Dr. Masaya Sawamura 《Angewandte Chemie (International ed. in English)》2016,55(36):10816-10820
Copper‐catalyzed enantioselective allyl–allyl coupling between allylboronates and either Z‐acyclic or cyclic allylic phosphates using a new chiral N‐heterocyclic carbene ligand, bearing a phenolic hydroxy, is reported. This reaction occurs with exceptional SN2′‐type regioselectivities and high enantioselectivities to deliver chiral 1,5‐diene derivatives with a tertiary stereogenic center at the allylic/homoallylic position. 相似文献
665.
Construction of Hexahydrophenanthrenes By Rhodium(I)‐Catalyzed Cycloisomerization of Benzylallene‐Substituted Internal Alkynes through C−H Activation 下载免费PDF全文
Yasuaki Kawaguchi Dr. Shigeo Yasuda Prof. Dr. Chisato Mukai 《Angewandte Chemie (International ed. in English)》2016,55(35):10473-10477
The treatment of benzylallene‐substituted internal alkynes with [RhCl(CO)2]2 effects a novel cycloisomerization by C(sp2)?H bond activation to produce hexahydrophenanthrene derivatives. The reaction likely proceeds through consecutive formation of a rhodabicyclo[4.3.0] intermediate, σ‐bond metathesis between the C(sp2)?H bond on the benzene ring and the C(sp2)?RhIII bond, and isomerization between three σ‐, π‐, and σ‐allylrhodium(III) species, which was proposed based on experiments with deuterated substrates. 相似文献
666.
A novel fabrication process was developed for a single silver nanowire using DNA metallization in a nanochannel, and the electrical properties of this nanowire were evaluated using electrochemical impedance spectroscopy. After being isolated using a nanochannel measuring 500 nm in depth and 500 nm in width, a single λDNA molecule was electrostatically stretched and immobilized between two electrodes separated by a gap of 15 μm by applying an AC voltage of 1 MHz and 20 Vp‐p. Then, naphthalene diimide molecules terminally‐labeled with galactose moieties were intercalated into the λDNA, and the reduction of silver ions along the λDNA led to its metallization with silver. Scanning electron microscopy observations revealed that two nanowires having different average widths of 154 nm and 250 nm were formed in two individual nanochannels. The nanowires showed the linear current‐voltage characteristics, and their combined resistance was estimated to be 45.5 Ω. The complex impedance of the nanowires was measured, and an equivalent circuit was obtained as a series connection of a resistance and a parallel resistance‐constant phase element circuit. Impedance analysis revealed that the nanowire included silver grain boundaries, and the bulk resistivity of silver grain was estimated to be 8.35×10?8 Ωm. 相似文献
667.
Dr. Shigeo Yasuda Yasuaki Kawaguchi Yuta Okamoto Prof. Dr. Chisato Mukai 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(34):12181-12188
A highly chemo‐ and regioselective partially intramolecular rhodium(I)‐catalyzed [2+2+2] cycloaddition of allenynes with alkynes is described. A range of diverse polysubstituted benzene derivatives could be synthesized in good to excellent yields, in which the allenynes served as synthetic equivalent to the diynes. A high regioselectivity could be observed when allenynes were treated with unsymmetrical alkynes. 相似文献
668.
π‐Electron Systems That Form Planar and Interlocked Anion Complexes and Their Ion‐Pairing Assemblies
Dr. Ryohei Yamakado Dr. Tsuneaki Sakurai Dr. Wakana Matsuda Prof. Shu Seki Dr. Nobuhiro Yasuda Prof. Shigehisa Akine Prof. Hiromitsu Maeda 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(2):626-638
Interactions between designed charged species are important for the ordered arrangements of π‐electron systems in assembled structures. As precursors of π‐electron anion units, new arylethynyl‐substituted dipyrrolyldiketone boron complexes, which showed anion‐responsive behavior, were synthesized. They formed a variety of receptor–anion complexes ([1+1] and [2+1] types) in solution, and the stabilities of these complexes were discussed in terms of their thermodynamic parameters. Solid‐state ion‐pairing assemblies of [1+1]‐ and [2+1]‐type complexes with countercations were also revealed by single‐crystal X‐ray analysis. In particular, a totally charge‐segregated assembly was constructed based on negatively and positively charged layers fabricated from [2+1]‐type receptor–anion complexes and tetrabutylammonium cations, respectively. Furthermore, the [1+1]‐type anion complex of the receptor possessing long alkyl chains exhibited mesophases based on columnar assembled structures with contributions from charge‐by‐charge and charge‐segregated arrangements, which exhibited charge‐carrier transporting properties. 相似文献
669.
Hiroyuki Shirahama Kiyoshi Mizuma Koichi Umemoto Hajime Yasuda 《Journal of polymer science. Part A, Polymer chemistry》2001,39(9):1374-1381
Homopoly(L ‐lactide) and homopoly(D,L ‐lactide) were almost inert for biodegradation with tricine buffer or normal enzymes such as bromelain, pronase, and cholesterol esterase but biodegradable with proteinase K. Significantly enhanced biodegradation was observed when an optically active (R)‐ or (S)‐3‐methyl‐4‐oxa‐6‐hexanolide (MOHEL) unit was introduced into poly(L ‐lactide) [poly(L ‐LA)] or poly(D,L ‐lactide) [poly(D,L ‐LA)] sequences. Poly[L ‐LA‐ran‐(R)‐MOHEL] in molar ratios of 86/14 to 43/57 showed good biodegradability that was independent of crystallinity. The biodegradation of polymers with proteinase K increased in the following order: poly[D,L ‐LA‐ran‐(R)‐MOHEL] > poly[L ‐LA‐ran‐(R)‐MOHEL] > poly[D,L ‐LA‐ran‐(S)‐MOHEL] > poly[L ‐LA‐ran‐(S)‐MOHEL] > poly(R)‐MOHEL > poly(D,L ‐LA). The number‐average molecular weight, molecular weight distribution, glass‐transition temperature, and melting temperature did not change before and after the biodegradation of poly[L ‐LA‐ran‐(R)‐MOHEL], indicating that the degradation occurred from the polymer surface. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 1374–1381, 2001 相似文献
670.
Tomohiro Yasuda Yukiko Okimura Arata Oishi Hisashi Kokubo Masayoshi Watanabe 《Journal of polymer science. Part A, Polymer chemistry》2013,51(10):2233-2242
The alternating copolymerization of phenylmaleimide (PMI) with a pendant sulfonamide acid group (sa‐PMI) and n‐butyl vinyl ether (BVE) as the aliphatic vinyl monomer afforded proton‐conducting polymer electrolytes—sa‐PMI‐BVEs—and their properties were compared with those of sa‐PMI‐STs that were synthesized from sa‐PMI and styrene. The ion exchange capacities (IECs) can be easily controlled by partly replacing sa‐PMI with unsubstituted PMI. sa‐PMI‐BVE is more flexible than sa‐PMI‐ST, and therefore, forms thin membranes even at high IECs, while sa‐PMI‐ST membranes are rigid and brittle. However, sa‐PMI‐BVE exhibits rather low thermal and oxidative stability. To realize polymer electrolyte membranes with reliable mechanical strength and a high IEC, gel‐filled membranes were prepared by polymerization in the presence of a small amount of a crosslinker, divinylbenzene, in porous polytetrafluoroethylene membranes. By using the gel‐filled membrane, H2/O2 fuel cells could be operated at 80 °C with reasonable performance. © 2013 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013 相似文献