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1.
Babij C Farrar DH Koshevoy IO Poë AJ Tunik SP 《Dalton transactions (Cambridge, England : 2003)》2005,(1):116-122
Reactions of the halides X- (X- = chloride, bromide or iodide) with the substituted cluster Rh6(CO)15(PPh3) in oxygen-free chloroform lead to [Rh5(CO)14(PPh3)]-, Rh(CO)2(PPh3)2X and [Rh(CO)2X2]- in the molar ratios 2:1: approximately 13. Oxidation by the solvent is assumed to lead to most of the Rh(I) product, and the stoichiometry for reactions with I- can be defined as 4Rh6(CO)15(PPh3) + 27I- + 12CHCl3 --> 2[Rh5(CO)14(PPh3)]- + Rh(CO)2(PPh3)2I + 13[Rh(CO)2I2]- + 6C2H2Cl4 + 4CO + 12Cl-. This can be rationalized quite simply with the aid of a few generally justifiable assumptions. Rate constants for reactions with bromide increase to a limiting value with increasing [Br-] in a way that shows that breaking of one Rh-Rh bond, with an unusual closo to nido structural change, is rate determining. This opening of the cluster might be spontaneous or solvent induced. To complete the reaction, the bromide has to compete with the reverse nido to closo change. The same closo to nido change is also a major rate determining step for reactions with P(OPh)3 in oxygen-free solutions, and for reactions with bromide in oxygenated solutions in the presence of trifluoroacetic and some other acids. The limiting rates increase slightly with increasing basicity of the ligands P(p-XC6H4)3 along the series X = F3C, Cl, F, H and MeO. Activation parameters for these reactions are reported. 相似文献
2.
S. P. Tunik S. I. Pomogailo G. I. Dzhardimalieva A. D. Pomogailo I. I. Chuev S. M. Aldoshin A. B. Nikol'skii 《Russian Chemical Bulletin》1993,42(5):937-942
Mono- and disubstituted cluster metal-containing monomers were obtained under mild conditions on interaction of Rh6(CO)16 with 4-vinylpyridine (4-ViPy) in the presence of N-trimethylaminoxide. These products were characterized by IR and1H NMR spectroscopy and by elemental and X-ray analyses. Rh6(CO)15(4-ViPy) was found to be an octahedral cluster with eleven terminal and four 3-bridging carbonyl ligands. 4-ViPy is linked with the Rh(3) atom through the N atom and occupies the coordination site of the twelfth CO terminal ligand. The mean value of the Rh-Rh bond length is 2.762 Å. The unsaturated ligand has little or no effect on the geometry of the starting cluster and its double bond retains the ability to undergo addition reactions.For part 28, seeRuss. Chem. Bull., 1993, 453.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 975–979, May, 1993. 相似文献
3.
Koshevoy IO Grachova EV Tunik SP Haukka M Pakkanen TA Heaton BT Iggo JA Podkorytov IS 《Dalton transactions (Cambridge, England : 2003)》2004,(22):3893-3899
Two novel heterometallic octahedral clusters [Rh(4)Pt(2)(CO)(11)(dppm)(2)](1) and [Ru(2)Rh(2)Pt(2)(CO)(12)(dppm)(2)](2) were synthesized by the reaction of [Rh(2)Pt(2)(CO)(6)(dppm)(2)] with [Rh(6)(CO)(14)(NCMe)(2)] and Ru(3)(CO)(12), respectively. Solid state structures of 1 and 2 have been established by a single crystal X-ray diffraction study. Two dppm ligands in 1 are bonded to one platinum and three rhodium atoms, which form an equatorial plane of the Rh(4)Pt(2) octahedron. Two rhodium and two platinum atoms bound to the diphosphine ligands in 2 are nonplanar to give an octahedral C2 symmetric Ru(2)Rh(2)Pt(2)(dppm)2 framework. The (31)P NMR investigation of and (1D, (31)P COSY, (31)P-[(103)Rh] HMQC) and simulation of 1D spectral patterns showed that in both clusters the structures of the M(6)(PP)(2) fragments found in the solid state are maintained in solution. 相似文献
4.
5.
Anastasia I. Solomatina Daria O. Kozina Vitaly V. Porsev Sergey P. Tunik 《Molecules (Basel, Switzerland)》2022,27(1)
Herein we report four [Ir(N^C)2(L^L)]n+, n = 0,1 complexes (1–4) containing cyclometallated N^C ligand (N^CH = 1-phenyl-2-(4-(pyridin-2-yl)phenyl)-1H-phenanthro[9,10-d]imidazole) and various bidentate L^L ligands (picolinic acid (1), 2,2′-bipyridine (2), [2,2′-bipyridine]-4,4′-dicarboxylic acid (3), and sodium 4,4′,4″,4‴-(1,2-phenylenebis(phosphanetriyl))tetrabenzenesulfonate (4). The N^CH ligand precursor and iridium complexes 1–4 were synthesized in good yield and characterized using chemical analysis, ESI mass spectrometry, and NMR spectroscopy. The solid-state structure of 2 was also determined by XRD analysis. The complexes display moderate to strong phosphorescence in the 550–670 nm range with the quantum yields up to 30% and lifetimes of the excited state up to 60 µs in deoxygenated solution. Emission properties of 1–4 and N^CH are strongly pH-dependent to give considerable variations in excitation and emission profiles accompanied by changes in emission efficiency and dynamics of the excited state. Density functional theory (DFT) and time-dependent density functional theory (TD DFT) calculations made it possible to assign the nature of emissive excited states in both deprotonated and protonated forms of these molecules. The complexes 3 and 4 internalize into living CHO-K1 cells, localize in cytoplasmic vesicles, primarily in lysosomes and acidified endosomes, and demonstrate relatively low toxicity, showing more than 80% cells viability up to the concentration of 10 µM after 24 h incubation. Phosphorescence lifetime imaging microscopy (PLIM) experiments in these cells display lifetime distribution, the conversion of which into pH values using calibration curves gives the magnitudes of this parameter compatible with the physiologically relevant interval of the cell compartments pH. 相似文献
6.
7.
Multiple-metal spin transitions which distort the HMQC spectra of rhodium carbonyl clusters are discussed. These effects are seen whenever the detector nucleus, e.g. 13C or 31P, couples to more than one metal spin and are not restricted to detector ligands occupying edge- or face-bridging sites. These effects are illustrated in, but not limited to, the 13C-{103Rh} and 31P-{103Rh} HMQC spectra of [Rh6(CO)15L], (where L = P(4-F-C6H4)3), [Rh4(CO)11{P(OPh)3}], [Rh6C(CO)15]2- and [Rh2(carboxylate)2PPh3]. The effect is to modulate the intensity and position of the correlations in the metal dimension; cross peaks are displaced from the true chemical shift, additional cross peaks are seen and the intensity of the coherences varies as a function of the preparation delay, d2, and coupling constant, and may go to zero at the conventional value of 1/(2J). Analyses of the relevant spin systems are given together with experimental strategies to overcome these effects. 相似文献
8.
Boris A. Trofimov Boris G. Sukhov Svetlana F. Malysheva Natal’ya A. Belogorlova Anatolii P. Tantsirev Lidiya N. Parshina Ludmila A. Oparina Sergey P. Tunik Nina K. Gusarova 《Tetrahedron letters》2004,45(49):9143-9145
Secondary phosphines react readily with a vinyl ether of diacetone-d-glucose under radical initiation conditions to give, in high yield, anti-Markovnikov adducts, diorganyl{2-[3-O-(1,2:5,6-di-O-isopropylidene)-d-glucofuranosyloxy]ethyl}phosphines, which oxidize almost quantitatively upon reacting with air oxygen or elemental sulfur to form the corresponding optically active phosphine oxides or sulfides. 相似文献
9.
Koshevoy IO Haukka M Selivanov SI Tunik SP Pakkanen TA 《Chemical communications (Cambridge, England)》2010,46(47):8926-8928
The assembly of the gold(I)-diphosphine cages occurs via unprecedented transformation of the alkynyls into the μ(4)-methylydine ligands under basic conditions. These compounds demonstrate the equilibrium between the P?M helical isomers and serve as hosts to accommodate small molecules (CH(2)Cl(2) and CS(2)). 相似文献