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91.
92.
Akasaka T Lu X Kuga H Nikawa H Mizorogi N Slanina Z Tsuchiya T Yoza K Nagase S 《Angewandte Chemie (International ed. in English)》2010,49(50):9715-9719
93.
94.
Infrared and electronic spectroscopy was applied to the benzene-ammonia cluster cation in the gas phase, and the observed spectra revealed the formation of a new C-N valence bond between the benzene and ammonia moieties, which has been predicted by the quantum chemical calculations (Tachikawa, H. Phys. Chem. Chem.Phys. 2002, 4, 6018). This cluster cation is regarded as a model for the cyclohexadienyl type intermediate in nucleophilic substitution reactions. 相似文献
95.
Wakahara T Nikawa H Kikuchi T Nakahodo T Rahman GM Tsuchiya T Maeda Y Akasaka T Yoza K Horn E Yamamoto K Mizorogi N Slanina Z Nagase S 《Journal of the American Chemical Society》2006,128(44):14228-14229
We show here that La@C72 has a non-IPR cage, unique electronic properties, and high reactivity by the spectroscopic and X-ray crystallographic analysis and the theoretical study. The isolation of La@C72 as a stable derivative might constitute an important stepping-stone on the way to isolation of these unknown metallofullerenes and open new material science of metallofullerenes. 相似文献
96.
Tsuchiya T Sato K Kurihara H Wakahara T Maeda Y Akasaka T Ohkubo K Fukuzumi S Kato T Nagase S 《Journal of the American Chemical Society》2006,128(45):14418-14419
Complexation behavior of the paramagnetic La@C82 metallofullerene with organic donor molecules (D) in solution is investigated. It is revealed that La@C82 and D form a 1:1 complex as a result of electron transfer. La@C82 and D are in equilibrium with [La@C82]-/[D]*+ in solution, which is readily controllable by changing the temperature and solvent. 相似文献
97.
Maeda Y Kanda M Hashimoto M Hasegawa T Kimura S Lian Y Wakahara T Akasaka T Kazaoui S Minami N Okazaki T Hayamizu Y Hata K Lu J Nagase S 《Journal of the American Chemical Society》2006,128(37):12239-12242
The dispersion of small-diameter single-walled carbon nanotubes (SWNTs) produced by the CoMoCAT method in tetrahydrofuran (THF) with the use of amine was studied. The absorption, photoluminescence, and Raman spectroscopies showed that the dispersion and centrifugation process leads to an effective separation of metallic SWNTs from semiconducting SWNTs. Since this method is simple and convenient, it is highly applicable to an industrial utilization for widespread applications of SWNTs. 相似文献
98.
An alanine-derived aminohydroxyphosphine ligand was developed for copper-catalyzed asymmetric conjugate addition of organozinc reagents to alpha,beta-unsaturated carbonyl compounds. This new tridentate ligand induces consistently high enantioselectivity in reactions of a variety of acyclic substrates. Theoretical mechanistic analysis suggests that the C-C bond formation takes place through a highly ordered transition state by the coordination of the phosphorus and nitrogen atoms to the copper(III) and zinc(II) atoms, respectively, and of the oxygen anion to both the metal centers. 相似文献
99.
Enantiomeric discrimination of chiral primary amines was performed by both reversed-phase HPLC and normal-phase HPLC after labeling with a chiral fluorescent derivatization reagent, (1R,2R)- and (1S,2S)-trans-2-(2,3-anthracenedicarboximido)cyclohexanecarbonyl chloride. Use of HPLC permits separation of diastereomeric derivatives of amines up to C30 which have a primary amino group at the middle of the alkyl chain. The derivatives of primary amines having an anteiso alkyl chain, which has a chiral branched-methyl at the n-3 position of the alkyl chain, were also separated by HPLC, and it was also possible to separate niphatesine D by reversed-phase HPLC after derivatization. 相似文献
100.
Naohiko Yoshikai Arimasa Matsumoto Jakob Norinder Eiichi Nakamura 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2009,121(16):2969-2972
Naheliegende Alternative : Eine eisenkatalysierte Imin‐gesteuerte C‐H‐Aktivierung mit einem Diarylzinkreagens führt eine Arylgruppe in ortho‐Stellung an einem von Acetophenon abgeleiteten Imin ein (siehe Schema); mit einem Palladiumkatalysator tritt dagegen eine gewöhnliche Substitution auf. Die Titelreaktion ist eine milde C‐H‐Aktivierung, die in Gegenwart von 1,2‐Dichlorisobutan mit Arylbromiden, ‐chloriden oder ‐sulfonaten selektiv verläuft.