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Catalytic epoxidation of olefin over supramolecular compounds of molybdenum oxide clusters and a copper complex 被引量:4
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作者 高洪成 颜岩 +5 位作者 徐晓弘 于杰辉 牛会玲 高文秀 张文祥 贾明君 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2015年第11期1811-1817,共7页
The catalytic epoxidation of olefin was investigated on two copper complex-modified molybdenum oxides with a 3D supramolecular structure, [Cu(bipy)]4[Mo15O47].2H2O (1) and [Cu1(bix)][(Cu1bix) (δ-MoVl8O26)0.... The catalytic epoxidation of olefin was investigated on two copper complex-modified molybdenum oxides with a 3D supramolecular structure, [Cu(bipy)]4[Mo15O47].2H2O (1) and [Cu1(bix)][(Cu1bix) (δ-MoVl8O26)0.5] (2) (bipy = 4,4'-bipyridine, bix = 1,4-bis(imidazole-1-ylmethyl)benzene). Both compounds were catalytically active and stable for the epoxidation of cyclooctene, 1-octene, and styrene with tert-butyl hydroperoxide (t-BuOOH) as oxidant. The excellent catalytic performance was attributed to the presence of stable coordination bonds between the molybdenum oxide and copper complex, which resulted in the formation of easily accessible Mo species with high electropositivity. In addition, the copper complex also acted as an active site for the activation of t-BuOOH, thus im- proving these copper complex-modified polyoxometalates. 展开更多
关键词 Supramolecular compound molybdenum oxide cluster Copper complex Olefin Epoxidation
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SYNTHESIS AND STRUCTURE OF TETRANUCLEAR MOLYBDENUM CLUSTER COMPOUND[Mo_4S_4(μ-O_2CC_6H_5)_2(dtp)_4]
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作者 Hong Hui ZHUANG Ding Ming WU Jian Quan HUANG Jin Ling HUANG Fuzhou Laboratory of Structure Chemistry and Fujian Institute of Research on the Structure of Matter,Chinese Academy of Sciences,Fuzhou 350002 《Chinese Chemical Letters》 SCIE CAS CSCD 1991年第7期553-554,共2页
The cluster compound[Mo_4S_4(μ-O_2CC_5H_5)_2(dtp)_4](dtp=S_2P(OEt)_2)was obtained by the ligand substitution reaction of tetranuclear molybdenum cluster [Mo_4S_4(μ-dtp)_2(dtp)_4]in the mixed solvent of acetone,ethan... The cluster compound[Mo_4S_4(μ-O_2CC_5H_5)_2(dtp)_4](dtp=S_2P(OEt)_2)was obtained by the ligand substitution reaction of tetranuclear molybdenum cluster [Mo_4S_4(μ-dtp)_2(dtp)_4]in the mixed solvent of acetone,ethanol and water in the presence of C_6H_5CO_2Na.It is monoclinic and crystallizes in space group C2/c, Mr=1495.09,a=12.175(5),b=22.01(1),c=20.875(9),β=99.04(4)°;V=5575(5);Z=4; Dc=1.78g/cm^3.Final R factor is 0.066.The result reveals that the[Mo_4S_4]cluster core and t-(dtp)^(-1)ligands are retained and only μ-bridged(dtp)^(-1)ligands are substituted by(C_6H_5CO_2)^(-1)in the substitution reaction,thus producing the new title cluster compound,the structure of which contains two species of bidentate ligand. 展开更多
关键词 MO DTP CO SYNTHESIS AND STRUCTURE OF TETRANUCLEAR molybdenum CLUSTER COMPOUND[Mo4S4 O2CC6H5 CC
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Synthesis and Structure of Dimolybdenum(I) Carbonyl Compound with Thiolate and Carboxylate Mixed-tri-bridging Ligands [Bu_4N][Mo_2(CO)_6(SC_6H_4Cl-p)_2(CF_3COO)]
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作者 潘国华 庄伯涛 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2001年第5期381-383,共3页
The crystal of the title compound with formula C36H44Cl2F3Mo2NO8S2 (Mr = 10002.62) crystallized in monoclinic, space group P21/n, with a = 9.6184(1), b = 22.3476(2), c = 20.7758(2) ?, ( = 90.172(1)(, V = 4465.70(7) ?3... The crystal of the title compound with formula C36H44Cl2F3Mo2NO8S2 (Mr = 10002.62) crystallized in monoclinic, space group P21/n, with a = 9.6184(1), b = 22.3476(2), c = 20.7758(2) ?, ( = 90.172(1)(, V = 4465.70(7) ?3, Z = 4, Dc = 1.491 g/cm3, F(000) = 2032, ( = 0.833 mm-1, Final R = 0.0665 and wR = 0.1650 for 5044 reflections with I >2.0( (I). The crystal structure revealed that the Mo2S2 core is planar, and the trifluoroacetic group acts as a bidentate bridging ligand and coordinates to two Mo atoms forming a five-membered ring plane, in which the Mo-Mo bond distance is 2.9222(9) ? and the O-C-O angle is 131.8(7) 展开更多
关键词 molybdenum(I) compound SYNTHESIS STRUCTURE Mo_2S_2 unit carboxylate ligand
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Synthesis and structure of an open-type trinuclear molybdenum cluster compound[Mo_3(μ_3-S)(μ-S)_2-(μ-OAc)(S_2CNC_4H_8)_3(O)_2]·0.5CH_2Cl_2·2H_2O
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作者 LU,Shao-Fang HUANG,Zi-Xiang Fujian Institute of Research on the Structure of Matter,Chinese Academy of Sciences,Fuzhoa,Fujian 350002 HUANG,Jian-Quan +1 位作者 ZHANG,Bin HUANG,Jin-Ling Department of Chemistry,Fuzhou University,Fuzhou,Fujian 350002 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1992年第1期52-58,共0页
The title compound was prepared by the reaction of Mo_3S_4(dtp)_4(H_2O)[ctp=S_2P(OEt)_2] with NaOAc·3H_2O and C_4H_8NCS_2NH_4.Crystallographic data:[Mo_3(μ_3-S)(μ-S)_2(μ-OAc)- (S_2CNC_4H_8)_3(O)_2]·0.5CH_... The title compound was prepared by the reaction of Mo_3S_4(dtp)_4(H_2O)[ctp=S_2P(OEt)_2] with NaOAc·3H_2O and C_4H_8NCS_2NH_4.Crystallographic data:[Mo_3(μ_3-S)(μ-S)_2(μ-OAc)- (S_2CNC_4H_8)_3(O)_2]·0.5CH_2CI_2·2H_2O,Mr=980.18,triclinic,space group P(?),α=12.360(3),b=16.653(6), c=9.206(2)A,α=101.97(2),β=108.32(2),γ=86.14(3)°.V=1759.6(9)A^3,Z=2,Dc=1.85 g/cm^3, F(000)=962,μ(Mo K_α)=16.53 cm^(-1).Final R=0.044 for 4301 reflections with I≥3σ(I).This compound may be regarded as a mixed-valent trinuclear molybdenum cluster{Mo_2(V)Mo(Ⅳ)(μ_3-S)(μ-S)_2- (μ-OAc)(S_2CNC_4H_8)_3(O)_2}.The Mo-Mo distances are 2.783(1),2.833(1)and 3.374(2)A in the Mo_3 non-equilateral triangle and there exist only two Mo-Mo bonds.The cluster was obtained by oxi- dation and ligand substitution of{Mo_3(μ_3-S)(μ-S)_3[μ-S_2P(OEt_2)][S_2P(OEt)_2]_3(H_2O)}. 展开更多
关键词 MO S2CNC4H8 Synthesis and structure of an open-type trinuclear molybdenum cluster compound[Mo3 OAC CNC type CH Cl
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Synthesis and structural characterization of a novel dimolybdenum(Ⅰ) compound with mixed-tribridging ligands:[Bu_4N][Mo_2(μ-SPh)_2(μ-Cl)(CO)_6]
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作者 潘国华 庄伯涛 +2 位作者 何玲洁 陈久桐 卢嘉锡 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2000年第5期745-750,共6页
A novel mixed-trib ridged dimolybdenum(Ⅰ) compound [Bu4N][Mo2(n-SPh)2(u-Cl)(CO)6] (1) has been synthesized from the reaction of Mo2 (CO)8 (SPh)2 with ButNCl.Compound 1 was characterized by IR,UV-Vis and 1H,13C,95Mo N... A novel mixed-trib ridged dimolybdenum(Ⅰ) compound [Bu4N][Mo2(n-SPh)2(u-Cl)(CO)6] (1) has been synthesized from the reaction of Mo2 (CO)8 (SPh)2 with ButNCl.Compound 1 was characterized by IR,UV-Vis and 1H,13C,95Mo NMR spectroscopic analyses.The electrochemical behavior was measured by cyclic voltammetry,indicating a quasi-reversible two-electron transfer in one step.The crystal structure determined by X-ray crystallography shows that 1 contains a [Mo2(u-S)2(u-Cl)]- core with a planar Mo2S2 unit and a Cl bridge.The Mo-Mo distance is 0.28709(7) nm,and the Mo-Cl-Mo angle is 66.44(4).A newface-sharing bioctahedral structure is discussed. 展开更多
关键词 molybdenum(Ⅰ) compound crystal structure Mo_2S_2 unit cofacial bioctahedral structure IR NMR CV
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MoS2 saturable absorber for single frequency oscillation of highly Yb-doped fiber laser 被引量:3
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作者 陆宝乐 原莉梅 +4 位作者 齐新元 侯磊 孙博 付盼 白晋涛 《Chinese Optics Letters》 SCIE EI CAS CSCD 2016年第7期70-74,共5页
In this Letter, a single-frequency fiber laser using a molybdenum disulfide (MoS2) thin film as a saturable absorber is demonstrated. We use a short length of highly Yb-doped fiber as the gain medium and a fiber fer... In this Letter, a single-frequency fiber laser using a molybdenum disulfide (MoS2) thin film as a saturable absorber is demonstrated. We use a short length of highly Yb-doped fiber as the gain medium and a fiber ferrule with MoS2 film adhered to it by index matching gel (IMG) that acts as the saturable absorber. The saturable absorber can be used to discriminate and select the single longitudinal modes. The maximum output power of the single-frequency fiber laser is 15,3 mW at a pump power of 130 mW and the slope efficiency is 15.3%. The optical signal-to-noise ratio and the laser linewidths are -60 dB and 5.89 kHz, respectively. 展开更多
关键词 Fiber lasers Fibers molybdenum compounds Optical signal processing Pumping (laser) Signal to noise ratio YTTERBIUM
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