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61.
S.P. Vila Nova H.J. Batista C. de Mello Donegá G.F. de Sá 《Journal of luminescence》2006,118(1):83-90
The complexes tris(4,4,4-Trifluoro-1-(1-naphthyl)-1,3-butanedionate) (2,2′-bipiridyl) Ln(III), Ln(tan)3bipy, where Ln(III)=Eu3+ and Gd3+ have been synthesized, characterized and their photophysical properties (absorption, excitation and luminescence spectra and emission quantum yield) investigated down to 4.2 K. The Eu(tan)3bipy complex has its molecular structure experimentally determined using X-ray crystallography and theoretically using the SMLC/AM1 method as well as their electronic singlet and triplet states were calculated, using the INDO/S-CI method with a point charge model to represent the Eu3+ ion, where two values were adopted, +3.0e and +3.5e, to investigate the imperfect shielding of the 4f shells. The so calculated +3.5e model electronic absorption spectrum and low lying triplet state energies agreed very well with the experimental ones. The emission quantum yield of the Eu3+ complex is quite low at room temperature, namely 7%, probably due to the too low lying triplet state, 19,050 cm-1, and increases by a factor of three when the temperature is lowered to 4.2 K. This strong thermal effect indicates the presence of a channel deactivating the main emitting state, what can be due to a LMCT state possibly lying in the same spectral region, as usually found in Eu3+ compounds. 相似文献
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IntroductionThebulkpreparation1ofC6 0 andC70 clusters(fullerenes)hasstimulatedawidevarietyofexperimentalandtheoreticalstudies .2 5Wehavesuccessfullyexaminedthestructures ,UV visiblespectraandthenonlinearthird orderopticalpolarizabilities (γ)ofC6 0 andC70 .6 ,7Byin troductionofsubstituents ,thecentrosymmetriesofC6 0 andC70 arebrokenandthesecond orderopticalnonlinearitiesareinduced .ThechargeseparationinsubstitutedC6 0whichleadstoenhancementofβvaluehasalsobeendis cussed .5Inrecentyears ,a… 相似文献
64.
用AM1,INDO/CI方法研究了C60与2-环己烯-1-酮和2-环庚烯-1-酮[2+2]环加成所得衍生物C_(66)H8O和C67H1O的结构。结果表明,两种衍生物的顺反异构体都只具有C1对称,C66H8O的顺式异构具有较低的能量和较小的偶极矩,C67H10的顺式并构体能量较低,但偶极矩较大,以优化构型为基础,计算加成产物的UV谱,对电子跃迁进行了理论指认,并分析了光谱移动的原因。 相似文献
65.
AMI semi-empirical method was used to optimize the barbituric acid derivatives substituted with glucosyl B1-5 (series B), and the thiobarbituric acid derivatives substituted with glucosyl T1-5 (series T). Based on the optimized structures, INDO/CI method was adopted to calculate the electronic spectra. Meanwhile, the second-order nonlinear optical (NLO) coefficients βμ were calculated with the sum-over-state (SOS) formula. The results show that when the number of glucosyl units was increased, |βμ| values of the barbituric and thiobarbituric acid derivatives were both enhanced, especially for thiobarbituric acid derivatives. It indicates that non-conjugated substituted group could also improve NLO properties of materials when the number of repeated units was increased. Additionally, the absorption bands appearing in UV area are consistent with the proper change of the number of glucosyl units, and consequently it can be concluded that the high transparencies of all systems were scarcely varied. 相似文献
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Equilibrium geometries and relative stabilities of 24 possible isomers for C78O4 based on C78 (C2v) were studied by intermediate neglect of differential overlap (INDO) calculations. It was indicated that the most stable geometry is 28,29,30,31,52,53,73,78‐C78O4, where three oxygen atoms are added to the same hexagon, through which the longest axis of C78 (C2v) goes, and the forth oxygen atom is added to the C(73)? C(78) bond intersected by the shortest axis of C78 (C2v), and epoxide structures are formed. Electronic spectra of C78O4 isomers were investigated based on the optimized geometries. The blue shift of the first absorption for 28,29,30,31,52,53,73,78‐C78O4 compared with that of C78 (C2v) was rationalized and nature of transition for the peaks discussed. © 2005 Wiley Periodicals, Inc. Int J Quantum Chem, 2006 相似文献
68.
稀土硝酸盐与双啮杂环胺配体α,α′联吡啶(bipy)的配合物研究不多.Hart 等合成了Ln(NO_3)_3(bipy)_2配合物;亦已解析了3个晶体结构:La(NO_3)_3(bipy)_2,Tb(NO_3)_3(bipy)_2,La(NO_3)3·bipy·2H_2O·(B-15-C-5)(B-15-C-5=苯并15-冠-5,).我们对La(NO_3)_3(bipy)_2的电子结构和化学键作过研究.本文利用自旋非限制适于稀土配合物计算的INDO方法研究了La(NO_3)_3·bipy· 相似文献
69.
巴比妥酸苯胺取代衍生物二阶非线性光学性质和电子光谱的INDO/CI研究 总被引:4,自引:0,他引:4
利用量子化学密度泛函理论(DFT)B3LYP方法,在6-31G~*基组下对巴比妥酸 苯胺取代衍生物体系BA1~BA5进行几何结构优化,以优化后的构型为基础,应用 INDO/CI方法进行电子光谱计算,并结合实验数据进行了分析,同时应用完全态求 和(SOS)公式计算二阶非线性光学(NLO)系数β_μ,设计的系列体系中β_μ最 大值可达到65.47×10~(-30)esu。进一步探讨了体系的共轭性和烷基取代基链的长 度对二者的影响,结果表明,体系的共轭程度越高,烷基取代基的链长度赵长,体 系β_μ值越大,而λ_max红移。 相似文献
70.