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21.
The temperature dependences of the integrated intensity and of the Knight shift of 199Hg NMR signals are measured for liquid and solid mercury introduced into porous carbon and silica gel. A decrease in the temperature of completion of crystallization and a small temperature hysteresis (from 4 to 9 K) between melting and crystallization are observed. The melting temperature of mercury in pores coincides with that in the bulk. The 199Hg NMR signal from crystalline mercury under the condition of restricted geometry is observed for the first time. It is established that the Knight shift for liquid and crystalline mercury in pores is smaller than in the bulk. 相似文献
22.
A series of novel star-shaped porphyrin-triarylamine conjugates were synthesized by palladium-catalyzed cross-coupling reactions. The spectroscopic and electrochemical studies show that pi-conjugation of the porphyrin core is extended to the triarylamine moieties. 相似文献
23.
Jia-Wen Yao Wei-Chiung Chi Jing-Hao Xu Gene-Hsiang Lee Michael Y. Chiang Bo-Rong Peng Nai-Cheng Lin Chiung-Chin Hu Lee-Shing Fang Guo-Qiang Li Yu-Chia Chang Tsong-Long Hwang Ping-Jyun Sung 《Tetrahedron》2019,75(11):1510-1516
A known briarane, brianthein W (1), along with four new hydroperoxybriaranes, briaviolides R–U (2–5), have been obtained from the octocoral Briareum violaceum. The absolute configuration of 1 was determined by X-ray analysis for the first time and the structures of briaranes 2–5 were established by spectroscopic methods. Bioactivity study showed that briarane 3 decreased the production of superoxide anions from human neutrophils. 相似文献
24.
Wu JY Chang CH Thanasekaran P Tsai CC Tseng TW Lee GH Peng SM Lu KL 《Dalton transactions (Cambridge, England : 2003)》2008,(44):6110-6112
A triangular metalloprism, [((CO)3Re(mu-2)Re(CO)3)3(mu3-1)2], self-assembled from Re2(CO)10, 2,4,6-tri-4-pyridyl-1,3,5-triazine (tpt, 1), and indigo (H2(2)), represents a fairly novel example of strong face-to-face pi-pi interactions between the central triazine rings of the tpt ligands that bow significantly inward distorting the prismatic structure. 相似文献
25.
A new porphyrin appended with four crown ether units at meso-positions via an acetylene bridge was synthesized and structurally characterized, and its complexation with a variety of metal and diammonium cations was investigated. 相似文献
26.
Yu-Pin Wang Hsien-Li Leu Tso-Shen Lin Gene-Hsiang Lee 《Journal of organometallic chemistry》2008,693(15):2615-2623
With copper(I) iodide as catalyst, σ-alkynyls, compounds (η5-C5H5)Cr(NO)2(CC-C6H5) (5), [(η5-C5H4)-COOCH3]Cr(NO)2(CC-C6H5) (10), and [(η5-C5H4)-COOCH3]W(CO)3(CC-C6H5) (13), were prepared from their corresponding metal chloride 1, 6 and 12. Structures of compound 3, 5 and 12 have been solved by X-ray diffraction studies. In the case of 5, there is an internal mirror plane passing through the phenylethynyl ligand and bisecting the Cp ring. The phenyl group is oriented perpendicularly to the Cp with an eclipsed conformation. The twist angle is 0° and 118.4° for -CC-Ph and two NO ligands, respectively. The orientation is rationalized in terms of orbital overlap between ψ3 of Cp, dπ of Cr atom, and π∗ of alkynyl ligand, and complemented by molecular orbital calculation. The opposite correlation was observed on the chemical shift assignments of C(2)-C(5) on Cp ring in compounds 6 and 12, using HetCOR NMR spectroscopy. The electron density distribution in the cyclopentadienyl ring is discussed on the basis of 13C NMR data and compared with the calculations via density functional B3LYP correlation-exchange method. 相似文献
27.
The synthesis of a series of ruthenium 1,5-disubstituted 1,2,3-triazolato complexes, 1,5-disubstituted 1,2,3-triazoles, and a triazolium salt is reported. Treatment of the ruthenium azido complex [Ru]-N3 ( 1 , [Ru] = (η5-C5H5)(dppe)Ru, dppe = Ph2PCH2CH2PPh2) with an excess of ethyl propiolate results in the formation of a mixture of the Z- and E-forms of zwitterionic N(1)-bound N(3)-ethyl acryl-4-carboxylate triazolato complexes [Ru]N3(CH=CHCO2Et)C2H(CO2) ( Z - 2 ) and ( E - 2 ). The arylation of 2 with aromatic bromides gives a series of cationic N(1)-bound N(3)-ethyl acryl-4-alkoxycarbonyl triazolato complexes {[Ru]N3(CH=CHCO2Et)C2H(CO2CH2R)}[Br] ( 3a , R = Ph ; 3b , R = C6F5; 3c , R = 4-C6H4CN, 3d , R = 2,6-C6H3F2) and the subsequent cleavage of the Ru-N bond of 3a–d gives 1,5-disubstituted 1,2,3-triazoles N3(CH=CHCO2Et)C2H(CO2CH2R) ( 4a , R = Ph; 4b , R = C6F5; 4c , R = 4-C6H4CN; 4d , R = 2,6-C6H3F2) and [Ru]-Br. A 1,2,3-triazolium salt [N3(CH=CHCO2Et)(CH2C6F5)C2H2][Br] ( 5 ) was formed by transformation of 4b in BrCH2C6F5/chloroform mixture. The structures of Z-3a and Z-5 were confirmed by single-crystal x-ray diffraction analysis and both complexes participate in non-covalent aromatic interactions in the solid-state structures which can be favorable in the binding of DNA/biomolecular targets and have shown great potential in the application of biologically active anticancer drugs. 相似文献
28.
Chih-Chieh Wang Ciao-Shin Tsai Gene-Hsiang Lee Su-Ying Chien Bo-Hao Chen Yu-Chun Chuang 《中国化学会会志》2023,70(5):1155-1167
Two d10 M(II) (M = Cd and Zn) coordination polymers (CPs) with chemical formulas, {[Cd(L1)(NCS)2(H2O)]⋅C2H5OH}n (1) , and {[Zn(L1)(NCS)2]⋅C2H5OH⋅0.5H2O}n (2) (L1 = 1,3,5-tris(4-pyridylsulfanylmethyl)-2,4,6-trimethylbenzene) were synthesized and structurally characterized by single-crystal x-ray diffraction method. In compound 1 , the coordination environment of Cd(II) ion is distorted octahedral bonded to three nitrogen donors from three L1 ligands located in a facial-position, two nitrogen donors from NCS− and one water molecule. The L1 acts as a bridge ligand with tris-monodentate coordination mode in a cis-cis-cis structural conformation, connecting the Cd(II) to form a two-dimensional (2D) zigzag-like layered metal-organic frameworks. Adjacent 2D layers are then arranged orderly in an ABAB manner to complete its three-dimensional (3D) supramolecular architecture. In compound 2 , the coordination environment of Zn(II) ion is distorted tetrahedral bonded to two nitrogen donors from two L1 ligands and two nitrogen donors from two NCS− ligands. The L1 acts as a bridge ligand with bis-monodentate coordination mode in a cis-cis-cis structural conformation, connecting the Zn(II) ions to form a one-dimensional (1D) zigzag-like polymeric chain. Adjacent chains are arranged orderly in an alternate ABAB manner to generate a 2D framework and then further arranged in an AAA manner to complete its 3D supramolecular architecture. The structural characterization as well as thermal-stability and solvents de-/ad-sorption behavior of 1 and 2 are studied and discussed in details. 相似文献
29.
Diaza-18-crown-6 appended dual 7-hydroxyquinolines; mercury ion recognition in aqueous solution 总被引:2,自引:0,他引:2
Ho ML Chen KY Wu LC Shen JY Lee GH Ko MJ Wang CC Lee JF Chou PT 《Chemical communications (Cambridge, England)》2008,(21):2438-2440
8,8'-(1,4,10,13-Tetraoxa-7,16-diazacyclooctadecane-7,16-diyl)bis(methylene)diquinolin-7-ol (TDBQ) was synthesized and proved to recognize Hg2+ via reducing Hg2+ to Hg+, forming a unique Hg(2)2+ - complex. 相似文献
30.
Tzeng BC Chiu TH Chen BS Lee GH 《Chemistry (Weinheim an der Bergstrasse, Germany)》2008,14(17):5237-5245
Ligands L1 and L2' (L1=N,N',N'-tris(4-pyridyl)trimesic amide, L2'=N,N',N'-tris(3-pyridinyl)-1,3,5-benzenetricarboxamide) belonging to an interesting family of tripyridyltriamides with C(3)-symmetry have been utilized to construct 3D porous or hydrogen-bonded frameworks. Through a novel single-crystal-to-single-crystal anion-exchange process, [Cd(L1)(2)(ClO(4))(2)](n) (1c) can be obtained from [Cd(L1)(2)Cl(2)](n) (1b) in the presence of ClO(4)(-) anions. This anion-exchange process is highly selective and only the substitution of Cl(-) by ClO(4)(-) or PF(6)(-) could be realized; Cl(-) was found not to be substituted by BPh(4)(-). This demonstrates that the exchange process depends on the size of the anions in relation to the size of the cavities in the host material (ca. 7.5 A). In addition, the anion-exchange properties of 1 b have also been investigated by means of powder X-ray diffraction (PXRD), elemental analysis (EA), and infrared absorption spectroscopy (IR). Structurally, [Zn(L1)(NO(3))(2)](n)(2) consists of a 2D coordination network with five-coordinate Zn(II) ions. Surprisingly, different trigonal-bipyramidal Zn(II) ions propagate to form distinct respective sheet structures, A and B, which are packed in an A-B-A-B manner in the crystal lattice, and these are hydrogen-bonded to give a 3D extended framework. The molecular structure of [CuI(L2')](n)(3) shows that the Cu(I) ion adopts a distorted tetrahedral geometry, and 3 also forms a 2D coordination network. Significantly, this 2D coordination network is further assembled into a remarkable 3D homochiral framework through triple hydrogen bonding and pi...pi interactions. All of these 3D coordination polymers and/or hydrogen-bonded frameworks are luminescent in the solid state, and their solid-state luminescent properties have been investigated at room temperature and/or at 77 K. 相似文献