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1.
A new dipeptide compound, (R)-2,4-dioxo-5-fluoro-1-[1-(methoxycarbonyl) ethylaminocarbonylmethyl]-1,2,3, 4-tetrahydropyrimidine (5-FUAPM), has been synthesized and identified by means of elemental analysis, IR, ^1H NMR and ^13C NMR spectra. The single crystal of compound 5-FUAPMoDMF was also obtained and characterized by DSC-TGA techniques. The crystal belongs to orthorhombic space group P212121 with the cell parameters: a= 0.4740(7) nm, b= 1.923(3) nm, c= 1.9229 nm, a=β=y=90°, V= 1.753 nm^3, Z=4, Dc= 1.312 g/cm^3, Mr=346.32, F(000)=728 and u=0.111 mm^-1. The final R and wR are 0.1378 and 0.2862, respectively. The result of the biological test showed that the compound 5-FUAPM has certain antitumor activities. 相似文献
2.
四种5-氟尿嘧啶二肽衍生物的合成、晶体结构和抗癌活性 总被引:2,自引:0,他引:2
合成了四种新的5-氟尿嘧啶(5-Fu)二肽衍生物, 它们的结构经过元素分析、IR、1H NMR和13C NMR的表征, 比旋光度[a]D的测定结果表明了它们之间的对映异构关系, 用X射线衍射法测定了其中一对对映异构的晶体结构3a (S)和3b (R), 生物活性测试的结果表明这四种化合物都具有一定的抑制活性, 并且R型产物比S型产物抑制率高. 研究了2a和3a与DNA在Au电极上相互作用的伏安行为, 比较了它们跟5-氟尿嘧啶与双链DNA发生相互作用的差别. 相似文献
3.
1-烷基-3-甲基咪唑双三氟甲基磺酰胺型离子液体(Cnmim][NTf2])被认为是最有希望用于核燃料循环中的分离试剂之一, 虽然其化学结构在辐照过程中变化不大, 但在受到γ辐照后会发生明显的变色, 因此有必要研究该类离子液体的变色原因. 本文以60Co为辐照源, 系统研究了辐照后不同C(1)-烷基链长和咪唑环上C(2)位上的H被甲基取代后离子液体的紫外-可见(UV-Vis)吸收光谱行为, 并结合辐照后离子液体荧光光谱和质谱的变化, 分析了导致该类离子液体辐照后颜色加深的原因. 结果表明, 随着咪唑环上C(1)―烷基链长度和剂量增大, 离子液体颜色加深; 而C(2)位上的H被甲基取代后颜色明显变浅. 辐照后咪唑型离子液体的变色主要来自于辐照后产生的烷基侧链含双键的咪唑阳离子, 咪唑阳离子二聚体和含氟咪唑化合物. 此外, γ辐照引起咪唑阳离子易发生π-π堆积, 而聚集态含量增加也会引起颜色加深. 相似文献
4.
二环己基-18-冠-6(DCH18C6)可以有效地从高放废液中分离90Sr,对于减小放射性废物的危害和实现高放废物的减容有重要意义.由于在实际应用中DCH18C6处于射线照射下,其结构可能会被破坏并引起络合能力的变化,因此有必要对该配合物的辐射稳定性进行研究.本文合成了Sr(NO3)2?DCH18C6配合物晶体,并通过单晶X射线衍射(XRD)与扩展X射线吸收精细结构谱(EXAFS)等方法进行了表征,确定Sr2+与周围氧原子的配位数为10,Sr―O平均键长约为0.268 nm/0.266 nm(XRD/EXAFS).配位原子来自DCH18C6的六个氧原子以及两个作为双齿配体的硝酸根的四个氧原子.对该配合物晶体在空气中进行γ辐照,EXAFS结果表明吸收剂量为400 kGy时,Sr―O键长及配位数没有发生变化,配位结构没有被破坏,具有很好的耐辐照稳定性.显微红外光谱(Micro-FTIR)结果进一步证明辐照后冠醚环的部分C―H键氧化为羟基或羰基,但并不影响DCH18C6与Sr2+的配位结构. 相似文献
5.
二茂铁(Ⅲ)鎓离子三氯乙酸盐对艾氏腹水癌细胞DNA合成的抑制郭茂林,杨频,赵春贵,杨斌盛,杨维萍(山西大学分子科学研究所,太原,030006)(山西煤炭中心医院肿瘤科)关键词二茂铁离子盐,抗癌剂,DNA金属茂类化合物抗癌活性及作用机理的研究是近年来比... 相似文献
6.
The symmetric Ti/Au bi-layer point electrodes have been successfully patterned on theβ-Ga;O;films which are prepared by metal–organic chemical vapor deposition(MOCVD)and theγ-Cu I films which are prepared by spin-coating.The fabricated heterojunction has a large open circuit voltage(Voc)of 0.69 V,desired for achieving self-powered operation of a photodetector.Irradiated by 254-nm ultraviolet(UV)light,when the bias voltage is-5 V,the dark current(Idark)of the device is 0.47 p A,the photocurrent(Iphoto)is-50.93 n A,and the photo-to-dark current ratio(Iphoto/Idark)reaches about 1.08×10;.The device has a stable and fast response speed in different wavelengths,the rise time(τr)and decay time(τd)are 0.762 s and 1.741 s under 254-nm UV light illumination,respectively.While theτr andτd are 10.709 s and7.241 s under 365-nm UV light illumination,respectively.The time-dependent(I–t)response(photocurrent in the order of10-10 A)can be clearly distinguished at a small light intensity of 1μW·cm;.The internal physical mechanism affecting the device performances is discussed by the band diagram and charge carrier transfer theory. 相似文献
7.
以硅胶为载体, 采用键合接枝法将2-(二苯膦基)乙基三乙氧基硅烷(DPPES)共价键合于硅胶表面, 制备了性能优良的硅胶键合型膦配体(以SiO2(PPh2)表示). 以SiO2(PPh2)为配体, Rh(acac)(CO)2 (acac:乙酰丙酮)为催化前体, 负载铑膦络合物催化剂(SiO2(PPh2)/Rh)在1-辛烯氢甲酰化反应中原位生成. 对生成的负载型催化剂和硅胶键合型膦配体进行了傅里叶变换红外(FTIR)光谱表征, 考察了膦/铑摩尔浓度比([P]/[Rh])、温度等因素对铑催化的长链1-辛烯氢甲酰化反应的影响. 结果表明, 膦/铑摩尔浓度比的增加能显著提高反应的成醛选择性, 降低铑的流失. 在[P]/[Rh]=12、363 K、2.0 MPa、1.5 h 的温和反应条件下, 1-辛烯转化率和成醛选择性分别可达98.4%和95.3%, 其催化活性与DPPES或三苯基膦(TPP)作配体时的均相铑催化相近. 催化剂循环4 次后, 反应活性无明显下降, 1-辛烯转化率均在97.0%左右, 经电感耦合等离子体原子发射光谱(ICP-AES)检测,有机相中铑流失低于0.1%. 相似文献
8.
A polynuclear complex [Cd(endc)(H2O)]n·nH2O (endc = endo-norbomene-cis5,6-dicarboxylate anion) has been synthesized by the hydrothermal reaction of cadmium nitrate tetrahydrate with endo-norbomene-cis-5,6-dicarboxylic acid in 1:1 molar ratio,and structurally characterized by single-crystal X-ray diffraction.It crystallizes in monoclinic,space group P21/c with a = 1.16471(7),b = 0.95334(7),c = 0.91109(9) nm,Z = 4,V= 1.01035(14)nm3,Dc.= 2.160 g/cm3,μ= 2.172 mm-1,F(000) = 648,R =0.0302 and wR = 0.0752.According to structural analysis,each Cd(Ⅱ) ion is coordinated to six O atoms from three endc anions and one water molecule,giving a distorted octahedral geometry.Two- dimensional layer arrangement of the title complex is constructed from the bridging nature of endc.It is worth notice that adjacent two-dimensional layers are joined together to form a three-dimensional supramolecular framework via intermolecular hydrogen bonding interactions. 相似文献
9.
Prof. Dr. Qian Miao Dr. Farzaneh Rouhani Dr. Hamed Moghanni-Bavil-Olyaei Dr. Kuan-Guan Liu Xue-Mei Gao Jing-Zhe Li Xiu-De Hu Prof. Dr. Zhi-Min Jin Prof. Mao-Lin Hu Prof. Ali Morsali 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(43):9518-9526
As redox-active based supercapacitors are known as highly desirable next-generation supercapacitor electrodes, the targeted design of two ferrocene-functionalized (Fc(COOH)2) clusters based on coinage metals, [(PPh3)2AgO2CFcCO2Ag(PPh3)2]2 ⋅ 7 CH3OH (SC1: super capacitor) and [(PPh3)3CuO2CFcCO2Cu(PPh3)3] ⋅ 3 CH3OH (SC2), is reported. Both structures are fully characterized by various techniques. The structures are utilized as energy storage electrode materials, giving 130 F g−1 and 210 F g−1 specific capacitance at 1.5 A g−1 in Na2SO4 electrolyte, respectively. The obtained results show that the presence of CuI instead of AgI improves the supercapacitive performance of the cluster. Further, to improve the conductivity, the PSC2 ([(PPh3)2CuO2CFcCO2]∞), a polymeric structure of SC2, was synthesized and used as an energy storage electrode. PSC2 displays high conductivity and gives 455 F g−1 capacitance at 3 A g−1. The PSC2 as a supercapacitor electrode presents a high power density (2416 W kg−1), high energy density (161 Wh kg−1), and long cycle life over 4000 cycles (93 %). These results could lead to the amplification of high-performance supercapacitors in new areas to develop real applications and stimulate the use of the targeted design of coordination polymers without hybridization or compositions with additive materials. 相似文献
10.
Jia-Bin Pan Xuan-Ge Zhang Yi-Fan Shi Ai-Cui Han Yu-Jia Chen Jing Ouyang Mao-Lin Li Prof. Qi-Lin Zhou 《Angewandte Chemie (International ed. in English)》2023,62(15):e202300691
Free carbene readily causes multiple side reactions due to its high energy, thus its asymmetric transformation is very difficult. We present here our findings of high-pKa Brønsted acid catalysts that enable free carbene insertion into N−H bonds of amines to prepare chiral α-amino acid derivatives with high enantioselectivity. Under irradiation with visible light, diazo compounds produce high-energy free carbenes that are captured by amines to form free ylide intermediates, and then the newly designed high-pKa Brønsted acids, chiral spiro phosphamides, promote the proton transfer of ylides to afford the products. Computational and kinetic studies uncover the principle for the rational design of proton-transfer catalysts and explain how the catalysts accelerate this transformation and provide stereocontrol. 相似文献