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51.
Jonathan R. Dilworth Chi-Tat Kan Raymond L. Richards Joan Mason Ian A. Stenhouse 《Journal of organometallic chemistry》1980,201(2):C24-C26
A useful criterion of linear or bent geometry at Nα of diazenido (-NαNβR) ligands is afforded by 15N NMR. A very large downfield shift (ca. 350 ppm) of the Nα resonance is reported for the “doubly-bent” diazenido ligands in [RhCl2(15NNC6H4R-4)(PPh3)2] (R = H or NO2) compared with the “singly-bent” diazenido ligands in trans-[MX(15N2R1)(dppe)2] (M = Mo or W, X = Cl or Br, R1 = Et or COMe), [ReCl2(15N2COC6H5)(C5H5N)(PPh3)2] and [RuCl3(15NNC6H5)(PPh3)2]. 相似文献
52.
Cowley AR Dilworth JR Nairn AK Robbie AJ 《Dalton transactions (Cambridge, England : 2003)》2005,(4):680-693
Reaction of the proligand Ph2PN(SiMe3)2 (L1) with WCl6 gives the oligomeric phosphazene complex [WCl4(NPPh2)]n, 1 and subsequent reaction with PMe2Ph or NBu4Cl gives [WCl4(NPPh2)(PMe2Ph)] (2) or [WCl5(NPPh2)][NBu4] (3), respectively. DF calculations on [WCl5(NPPh2)][NBu4] show a W=N double bond (1.756 A) and a P-N bond distance of 1.701 A, which combined with the geometry about the P atom suggests, there is no P-N multiple bonding. Reaction of L1 with [ReOX3(PPh3)2] in MeCN (X = Cl or Br) gives [ReX2(NC(CH3)P(O)Ph2)(MeCN)(PPh3)](X = Cl, 4, X = Br, 5) which contains the new phosphorylketimido ligand. It is bound to the rhenium centre with a virtually linear Re-N-C arrangement (Re-N-C angle = 176.6 degrees, when X = Cl) and there is multiple bonding between Re and N (Re-N = 1.809(7) A when X = Cl). The proligand Ph2PNHNMe2(L2H) reacts with [(C5H5)TiCl3] to give [(C5H5)TiCl2(Me2NNPPh2)] (6). An X-ray crystal structure of the complex shows the ligand (L2) is bound by both nitrogen atoms. Reaction of the proligands Ph2PNHNR2[R2 = Me2 (L2H), -(CH2CH2)2NCH3 (L3H), (CH2CH2)2CH2 (L4H)] with [{RuCl(mu-Cl)(eta6-p-MeC6H4iPr)}2] gave [RuCl2(eta6-p-MeC6H4iPr)L] {L = L2H (7), L3H (8), L4H (9)}. The X-ray crystal structures of 7-9 confirmed that the phosphinohydrazine ligand is neutral and bound via the phosphorus only. Reaction of complexes 7-9 with AgBF4 resulted in chloride ion abstraction and the formation of the cationic species [RuCl(6-p-MeC6H4iPr)(L)]+ BF4- {(L = L2H (10), L3H (11), L4H (12)}. Finally, reaction of complex 6 with [{RuCl(mu-Cl)(eta6-p-MeC6H4iPr)}2] gave the binuclear species [(eta6-p-MeC6H4iPr)Cl2Ru(mu2,eta3-Ph2PNNMe2)TiCl2(C5H5)], 13. 相似文献
53.
Mixed-ligand Complexes of Technetium. XV. The Reaction of [TcNCl2(Me2PhP)3] with Dialkyldithiocarbamates and N,N-Dialkylthio-carbamoylbenzamidines [TcN(Cl)(Me2PhP)2(Et2dtc)], [TcN(Me2PhP)(Et2dtc)2], and [TcN(Et2dtc)2] can be prepared by stepwise ligand exchange reactions starting from dichlorotris(dimethylphenylphosphine)nitridotechnetium(V), [TcNCl2(Me2PhP)3], and diethyldithiocarbamate. In contrast to this, only one intermediate, [TcN(Cl)(Me2PhP)2(HEt2tcb)], could be isolated during the reaction with N,N-Diethlthiocarbamoylbenzamidine, which yields the bis chelate [TcN(HEt2tcb)2]. [TcN(Me2PhP)(Et2dtc)2] crystallizes in the monoclinic space group P21/c; a = 17.369(5) Å, b = 15.024(1) Å, c = 9.906(3) Å, β = 76.47(1)º, Z = 4. The phosphine is coordinated equatorially. The multiply bonded nitrogen ligand (Tc? N(1) 1.624(3) Å) strongly labilizes the trans positioned donor atom (distance Tc? S(4) 2.826(1) Å). [TcN(HEt2tcb)2] crystallizes in the triclinic space group P1 with a = 9.749(4) Å, b = 11.264(4) Å, c = 12.359(4) Å, α = 75.34(2)º, β = 79.69(2)º, γ = 87.55(2)º, Z = 2. The metal is five-coordinate with the nitrido donor atom occupying the apex of a square pyramid. It's basal plane is formed by the cis-coordinated chelate ligands. The technetium is situated over the basal plane by about 0.6 Å. The Tc?N distane was found to be 1.610(5) Å. 相似文献
54.
Tong LH Wong YL Pascu SI Dilworth JR 《Dalton transactions (Cambridge, England : 2003)》2008,(35):4784-4791
A new family of N-capped tripodal NO(3) proligands N,N-bis(2-hydroxy-3,5-di-tert-butylbenzyl)-N-(2'-hydroxy-5'-R-phenyl)amine [H(3)(L(n))] [when R= Me, n = 1; R= (t)Bu, n = 2; R = Cl, n = 3] with different substituents in one of the aryl rings and N,N-bis(2-hydroxy-3-tert-butylbenzyl)-N-(2'-hydroxy-5'-methylphenyl)amine [H(3)(L(4))] were synthesised. The preparation of a new pentadentate proligand N-methyl-N,N',N'-tris(2-hydroxy-3,5-di-tert-butylbenzyl)ethane-1,2-diamine [H(3)(L(5))] with an N(2)O(3) donor set is also reported. Reaction of the proligands [H(3)(L(n))] (n = 1-4) with iron(iii) chloride in the presence of base (triethylamine) and 1-methylimidazole (1-Meim) as co-ligand led to the formation of iron complexes of the type [Fe(L(n))(1-Meim)] (n = 1-4) () respectively, while treatment of the trilithium salt of [H(3)(L(5))] with iron(iii) chloride afforded [Fe(L(5))] (). All complexes were structurally characterised by X-ray crystallography. In complexes , the ligands form five- and six-membered chelate rings with the iron centres which have distorted trigonal bipyramidal geometry with an N(2)O(3) coordination environment. Complex adopts a similar distorted trigonal bipyramidal geometry also with N(2)O(3) coordination around the iron centre. The catalytic activity of these iron complexes towards epoxidation of styrene was examined. 相似文献
55.
S. J. Dilworth Denka Kutzarova Karen L. Shuman V. N. Temlyakov P. Wojtaszczyk 《Journal of Fourier Analysis and Applications》2008,14(5-6):609-628
We study the convergence of certain greedy algorithms in Banach spaces. We introduce the WN property for Banach spaces and prove that the algorithms converge in the weak topology for general dictionaries in uniformly smooth Banach spaces with the WN property. We show that reflexive spaces with the uniform Opial property have the WN property. We show that our results do not extend to algorithms which employ a ‘dictionary dual’ greedy step. 相似文献
56.
S. J. Dilworth E. Odell T. Schlumprecht A. Zsák 《Foundations of Computational Mathematics》2008,8(6):703-736
Let (e
i
) be a dictionary for a separable infinite-dimensional Banach space X. We consider the problem of approximation by linear combinations of dictionary elements with quantized coefficients drawn
usually from a ‘finite alphabet’. We investigate several approximation properties of this type and connect them to the Banach
space geometry of X. The existence of a total minimal system with one of these properties, namely the coefficient quantization property, is shown to be equivalent to X containing c
0. We also show that, for every ε>0, the unit ball of every separable infinite-dimensional Banach space X contains a dictionary (x
i
) such that the additive group generated by (x
i
) is (3+ε)−1-separated and 1/3-dense in X.
相似文献
57.
Density functional theory (DFT) calculations have been performed using the uB3LYP/6-31++G(d,p) model to calculate the solution phase one-electron reduction potentials (E(calc)) and absolute pKa values of a series of copper bis(thiosemicarbazonato) complexes. The effects of solvation in water and dimethylsulfoxide (DMSO) are incorporated as a self-consistent reaction field (SCRF) using the integral equation formalism polarisable continuum model (IEFPCM) and are found to be essential for quantitative agreement with an average error in E(calc) of -0.02 V compared to experiment. The bonding and spin densities are examined through the use of Natural Bond Order analysis and the results used to rationalise the calculated and observed reduction potentials. Calculated estimates of pKa values of several copper(II) species are presented and their implications for the mechanisms of transport and trapping within hypoxic cells are considered. Reduction is found to be a prerequisite for protonation of the complexes which suggests their transport in the blood stream as neutral species, and the mechanistic sequence is identified as a sequential electrochemical-chemical (EC) process. The complex equilibria of protonation, reoxidation and dissociation are discussed and the copper(I) diprotonated, cationic complex of diacetyl bis(4-methyl-3-thiosemicarbazonato)copper(II), Cu(I)ATSMH2(+), is identified as a possible candidate for the initial species trapped in hypoxic cells. 相似文献
58.
59.
We consider problems concerning the partial order structure of the set of spreading models of Banach spaces. We construct
examples of spaces showing that the possible structure of these sets include certain classes of finite semi-lattices and countable
lattices and all finite lattices.
Research of the second named author was partially supported by the National Science Foundation.
The third named author had a visiting appointment at the University of South Carolina for the 2004–05 academic year during
part of his research. 相似文献
60.
Arrowsmith RL Waghorn PA Jones MW Bauman A Brayshaw SK Hu Z Kociok-Köhn G Mindt TL Tyrrell RM Botchway SW Dilworth JR Pascu SI 《Dalton transactions (Cambridge, England : 2003)》2011,40(23):6238-6252
New fluorescent and biocompatible aromatic Ga(III)- and In(III)-bis(thiosemicarbazonato) complexes for dual mode optical and PET or SPECT molecular imaging have been synthesised via a synthetic method based on transmetallation reactions from Zn(II) precursors. Complexes have been fully characterised in the solid state by single crystal X-ray diffraction and in solution by spectroscopic methods (UV/Vis, fluorescence, (1)H and (13)C{(1)H} NMR). The bis(thiosemicarbazones) radiolabelled rapidly in high yields under mild conditions with (111)In (a gamma and Auger emitter for SPECT imaging and radiotherapy with t(1/2) = 2.8 d) and (68)Ga (a generator-available positron emitter for PET imaging with t(1/2) = 68 min). Cytotoxicity and biolocalisation studies using confocal fluorescence imaging and fluorescence lifetime imaging (FLIM) techniques have been used to study their in vitro activities and stabilities in HeLa and PC-3 cells to ascertain their suitability as synthetic scaffolds for future multimodality molecular imaging in cancer diagnosis and therapy. The observation that the indium complexes show certain nuclear uptake could be of relevance towards developing (111)In therapeutic agents based on Auger electron emission to induce DNA damage. 相似文献