SYNTHESIS AND CHARACTERIZATION OF (PPh_3)_3Co(μ-CO)_2 V(CO)_2Cp AND (PPh_3)

ＳＹＮＴＨＥＳＩＳＡＮＤＣＨＡＲＡＣＴＥＲＩＺＡＴＩＯＮＯＦ（ＰＰｈ_３）_３Ｃｏ（μ－ＣＯ）_２Ｖ（ＣＯ）_２ＣｐＡＮＤ（ＰＰｈ_３）ＨＰｔ（μ－ＣＯ）（μ－ＰＰｈ_２）Ｖ（ＣＯ）_２ＣｐＣｈａｎｇＰｉｎｇＳＨＡＯ（ＤａｌｉａｎＩｎｓｔｉｔｕｔｅｏｆＣｈ?..     

SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF TRIPYRRANE-CONAINING BISMACROCYCLE

ＳＹＮＴＨＥＳＩＳＡＮＤＳＴＲＵＣＴＵＲＡＬＣＨＡＲＡＣＴＥＲＩＺＡＴＩＯＮＯＦＴＲＩＰＹＲＲＡＮＥ－ＣＯＮＡＩＮＩＮＧＢＩＳＭＡＣＲＯＣＹＣＬＥ￥ＳｈｉＭｉｎｇＤＯＮＧ；ＤｕｏＹｕａｎＷＡＮＧ（ＩｎｓｔｉｔｕｔｅｏｆＰｈｏｔｏｇｒａｐｈｉｃＣｈｅｍ...     

[(O)MoCu_3(μ_3-S)_3(μ_3-Cl)(PPh_3)_3]·2THF的合成及其晶体结构

固体化合物(NH_4)_6Mo_7O_(24)·4H_2O和(PPh_3)_2CuCl与饱和液体NH_4HS反应获得桔红针状标题晶体。晶体空间群为P2_1/c,晶胞参数a=11.742(2),b=28.186(7),c=19.304(3),β=100.57(2)°,V=6280.4(?)~3,D_c=1.46g/cm~3,Z=4,F(000)=2816。在3≤2θ≤45°范围内收集到8414个独立衍射强度数据,其中3856个I≥1.5σ(I)强度数据参加结构计算。标题化合物分子是以{MoCu_3S_3Cl}类立方烷型簇为核心的分子,Mo—Cu的平均距离为2.716。     

SYNTHESIS AND CRYSTAL STRUCTURE OF [(PPh_3)_3(Cu_3S_3MoBr)O]-0. 5CH_2C1_2

<正> [(Ph3P)3 (Cu3S3MoBr)O] 0. 5CH2C12, Mr = 1308. 00, monoclinic, P21/c,a=11. 831(3),b = 28. 471(8),c=19. 232(5) A ,β= 101. 05(3)°,V = 6358 A3,Z = 4,DC=1.37 g/cm3,F(000) = 2620,μ(MoKa) = 20. 47 cm-1. Final R=0. 085 for 4271 observede reflections. The core [Cu3S3MoBr] has a distorted cubic configuration. Two dichloromethane molecules distribute statistically in a unit cell.     

STUDY OF ELECTROCHEMISTRY OF TETRANUCLEAR MOLYB-DENUM CLUSTER COMPOUND [Mo_4S_4(μ-dtp)_2(dtp)_4]

<正> The electrochemical behavior of tetranuclear molybdenum cluster [Mo4S4 (μ-dtp)2 (dtp)43 (1) (dtp = S2P (OEt)2) has been investigated by cyclic voltammetry, potentiotatic polarization measurement, controlled potential coulometry and pulse polarography. It is demonstrated that the compound undergoes two consecutive near reversible one-electron reductions at 0. 01V and -0. 77V , respectively and a near reversible one-electron oxidation at 1. 01V with scan rates from 25mV/sec to 1V/sec in cyclic voltammetric measurements. The cluster compound displays three redox processes, indicating its high structural stability.     

THE SYNTHESIS AND STRUCTURE OF THE CLUSTER COMPOUND {(Mo_3(μ_3-O)(S_2)_3[S_2P(OEt)a]3)2Cl}FeCl_4

<正> INTRODUCTION. Resently a series of M2-type trinuclear Mo clusters with the formula {Mo_3(μ-Y)(S_2)_3[S_2P(OEt)_2]_2]_3}X, (Y=O or S; X=Cl or I) have been synthesized by our research group through either the reduction of the higher valence Mo(V) compounds or the oxidation of the middle valence Mo(Ⅲ) species. In this paper we report a novel type of cluster cation     

RESEARCH ON TRINUCLEAR MOLYBDENUM CLUSTER COMPOUNDS——CRYSTAL AND MOLECULAR STRUCTURE OF Mo_3(μ_3—O)(μ_2—S_2)_3[S_2P(OEt)_2]_3I

The title crystals are golden yellow rhomboic plates, belonging to the monoelinic system. The space group is P_(B_1)/n with unit cell parameters a=16.570(2), b=12.370(1), c=20.007(2), β=99.97(1)°, Z=4, D_c=1.938 g.cm~(-3). The crystal structure was solved mainly by the heavy atom method and refined by the full-matrix least-squares to a final R factor of 0.047 based on 4387 unique reflections with intensities I≥2σ(I). The results show that the crystal structure consists of neutral mono-oxo-capped trinuclear molybdenum cluster molecules with an average Mo-Mo bond length of 2.626(4) and an average Mo-O bond length of 2.036(2) respectively. Each pair of Mo atoms is further bridged by an S_2~(2-) radical, in which one S atom is essentially situated on the triangular plane formed by these three Mo atoms and the other one is situated on the side of the plane opposite to the μ_3-O atom. Besides, each Mo atom is coordinated to two S atoms belonging to an [S_2P(OEt)_2]~-radical so as to complete a nearly pen     

SYNTHESIS AND CRYSTAL STRUCTURE OF Mo_3(μ_3-O)(μ-S)_3[S_2P(OEt)_2]_4(C_3H_3N_2)

<正> Mr=1164, space group C2/c, a=14.954(13)A,b=22.323(6)A,c=27.003(18)A,β=98.23(7)°,V=8920 A3, Z=8. Final R=0.069 for 2818 unique diffraction data with I≥30(I). The title cluster compound is of Ml configuration with a triple bridging atom O and with a 'loosely coordinated site' occupied by an imidazole ligand. Three Mo-Mo bond lengths are 2.657 (2), 2.649(2),and 2.646(2)A,respectively. The average bond length of Mo-(μ3-O) bonds is 2.052 A.     

SYNTHESIS AND CRYSTAL STRUCTURE OF A TUNGSTEN-COPPER-SULFUR CLUSTER [Et_4N]_2[WCU_3S_4(S_2CNEt_2)_3]

<正> [Et4N]2 [WCu3S4 (S2CNEt2)3], Mr = 1172. 01, orthorhombic, space group P212121 with a=12. 858(9),b=13. 204(5) ,c=29. 501(9) A ,V=5008. 7 A3, Z = 4, Dc = 1. 55gcm-3, μ(MoKa) = 40. 3cm-1. The final R and Rw are 0. 069 and 0. 075, respectively, for 3072 observed unique reflections. The anion contains a slightly distorted WS42~ tetrahedron coordinated by three CuS2 CNEt2 units,with four metal atoms lying in a plane.     

SYNTHESIS AND STRUCTURE OF COMPLEX(PPh3)_2Ni[S_2C=C(CN)_2]

(PPh_3)_2Ni(i-mnt),(i-mnt=S_2C=C(CN)_2),Mr=613.43,monoclinic,Pn,a=9.167(3),b=10.872(3),c=18.209(7) ,β=101.46(3)°,V=1779(1) ,Z=2,Dc=1.15 g/cm~3,λ(Moka)=0.71069 ,μ=7.67 cm~(-1),F(000)=648,T=296K,final R=0.060,Rw=0.073 for 1909 observed reflections with Ⅰ≥3σ(Ⅰ).The complexadopts a square planar geometry as its coordination unit,the mean Ni-S and Ni-P distances are 2.216and 2.221 ,respectivety.     

DESULPHURIZATION THROUGH THE CLEAVAGE OF C-S BOND-PREPARATION AND STRUCTURAL CHARACTERIZA-TION OF THE HEXACOBALT CLUSTER,[Co_6(μ_3-S)_8(PPh_3)_6]·2DMF·CH_3OH

<正> The crystal of cluster [Co6(μ3-S)8(PPh3)6] 2DMF CH3OH(1)was obtained by the reaction of CoCl(PPh3)3 with Na2pdt(H2pdt=1,2-propanedithiol)in methanol,and grown from DMF.The compound 1,C116H112 Co6N2O2P6S8(Mr=2362.11)is monoclinic,space group C2/c with cell parameters a=27.060(10),b=15.127(2),c=27.017(2)A,β=98.52(2)°,V=10937.0A3,Z=4,Dc=1.434 g/cm3,F(000)=4864,MoKa=11.716cm-1,final R=0.071 for 4134 independent reflections with I>3o(I).The cluster[Co6(μ3-S)8(PPh3)6] possesses crystallographic symmetry C2,and the inner Co6 core is a slightly distorted octahedron with all faces symmetrically capped by triply-bridging sulphur atoms.     

SYNTHESIS AND STRUTURE OF THE FIRST INTERSTITIAL μ_7-S CLUSTER Co_7(μ_7-S)(μ_4-PSEt)(μ-SEt)_2(μ-CO)_2(CO)_(12)

The reaction of Co_2(CO)_8 with EtSPCl_2 gives a new crystal like compound Co_7(μ_7-S)(μ_4-PSEt)(μ-SEt)_2(μ-CO)_2(CO)_(12),whose structure has been determined by single crystal x-ray diffraction.This special com-pound reveals some new features in cluster chemistry~1:The fragmentation of a ligand precursor EtSPCl_2 yieldsthree kinds of fragments,μ_7-S,μ_4-PSEt and μ-SEt,which are ligands in the same cluster molecule.There is anew type of bridging S presented——A μ_7-S atom is interspaced into seven Co core.     

SYNTHESIS AND STRUCTURE OF THE CLUSTER COMPOUND {[Mo_3(μ_3-S)(μ-S_2)_3(dtp)_3]_2Cl}·FeCl_4, (dtp=S_2P(OC_2H_5)_2)

<正> The title compound, C24H6oCl5O12P6S26FeMo6,Mr = 2369. 00,crystallized in monoclinic,space group P21/n with cell parameters a= 17. 378(9) ,b=19. 752 (6),c=23. 845(A),β=84. 50(4)°,V = 8133. 4A3,Z=4,Z)c=1.931gcm-3,F(000) = 4676. 00. MoKa radiation (λ=0. 71073A),R=0. 070 for 8403 reflections with I≥3σ(I). The structure was solved by direct methods and showed to consist of an anion Fe-Cl4- and a cluster cation {[Mo3(μ3-S) (S2)3 (dtp)3]2Cl} + which is a double-trinuclear molybdenum cluster formed by sharing a chlorine atom with six weak Cl -S bonds of about 2.936-3. 145A.     

THE SYNTHESIS AND CRYSTAL STRUCTURE OF Mo_3(μ_3-O)-(μ-S)_3(μ-OOCCH_3)(dtp)_3(Py)

<正> The title compound was obtained by the reaction of Mo3(μ3-O) (μ-S)3(dtp)4(H2O) with CH3COONa and pyridine. Mo3C19H38N1O9P3S9,Mr= 1093. 79, triclinic, space group P1, a = 12. 921(3) , b = 14. 260(3) , c= 12. 800(3)(?),α = 97. 54(2), β=116. 66(1), γ=100. 10(2) °, V = 2015, 2(8)(?)3, Z=2, Dc = 1. 80gcm-3, F(000) = 1092, final R = 0. 066 for 3444 observations, room temp. In the structure the three Mo atoms form an isosceles triangle capped by a μ3-O atom with three sides of 2. 589(2) , 2. 642(2), and 2. 627(2) (?) respectively, and the car-boxyl bridged Mo-Mo bond is the shortest one.     

STUDY OF REDOX PROPERTIES OF TETRANUCLEAR DENUM CLUSTER COMPOUND {Mo_4(μ_3-S)(μ_3-O)[S_2P(OEt)_2]_6}

<正> The redox properties of tetranuclear molybdenum cluster {Mo4(μ3-S)3(μ3-O)CS2P(OEt)2D6}(1)have been investigated by linear sweep voltammetry,cyclic voltammetry,differential pulse voltammetry and controlled potential coulome-try.It is showed that the compound undergoes two consecutive near reversible one-electron reductions at-0.03V and-0.79V respectively and a near reverisble one-electron oxidation at 0.98V with scan rates from 25 mV/sec to 1V/sec in cyclic voltammetric measurements.Three stable peaks can still be seen after several hours of repeated slow speed scan(1mV/sec)in differential pulse voltammetry.These evidences suggest the high structural stability of this cluster compound.     

RESEARCH ON TRINUCLEAR MOLYBDENUM CLUSTER COMPOUNDS——CRYSTAL AND MOLECULAR STRUCTURE OF Mo_3(μ_3-S)(μ_2-S_2)_3[S_2P(OEt)_2]_3Cl

The title crystal is straw-yellow in colour, belonging to the triclinic system. The space group is P with the following unit cell parameters:a=11.570(2), b=13.093(1), c=14.399(2), α=102.62(1), β=102.15(1), γ=111.87 (1)°, V=1870(1), Z=2, D_(calc)=1.960g·cm~(-3).The crystal structure was solved by the heavy atom method and refined by full-matrix least-squares to a final conventional R factor of 0.055. The results show that the crystal structure consists of neutral trinuclear Mo cluster molecules, in which three independent Mo atoms form an equilateral triangle with an average side length of 2.725(3), corresponding to a Me-Me single bond. On one side of the triangle one μ_3-S atom binds the three Mo atoms together to form a monoeapped trinuclear cluster. In addition, three S_2 radicals acting as μ_2 bridges are located between each two Mo atoms. Each Mo atom is also coordinated to two terminal S atoms of an [S_2P(OEt)_2]~- radical so as to complete a distorted pentagonal bipyramid configuration.     

SYNTHESIS AND CRYSTAL STRUCTURE OF COMPLEX [CrMo_3 (μ_3-O)_3(μ-O)(μ-O_2CCH_3)_5(O_2CCH_3)_3]Na2 · H_2O

<正> The title complex C CrMo3 (μ3-O )3 (μ-O) (μ-O2CCH3 )5 (O2CCH3)3]2Na2 · H2O (Mr=1814. 32) crystallizes in monoclinic, space group P21/ n with a=11.209(5), b=18. 05(1), c=14. 44(1) A , β= 98. 30(5)°. V=2890 (3) A3, Z=2, A = 2. 08 g/cm3, F(000) -1780, Final R = 0. 049, Rw = 0. 058 for 2622 independent reflectons with I>3σ(I). The complex anion contains two Mo3O4 cores which connect two chromium atoms through four μ3-O atoms and eight bridging CH3COO- groups. Each of the Cr atoms and the Mo atoms is coordinated by six oxygen atoms. The anions are linked by Na cations to form one-dimensional infinite chain structure.     

SYNTHESIS AND STRUCTURE OF TETRANUCLEAR MOLYBDENUM CLUSTER COMPOUND[Mo_4S_4(μ-O_2CC_6H_5)_2(dtp)_4]

The cluster compound[Mo_4S_4(μ-O_2CC_5H_5)_2(dtp)_4](dtp=S_2P(OEt)_2)wasobtained 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 thepresence 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]clustercore and t-(dtp)~(-1)ligands are retained and only μ-bridged(dtp)~(-1)ligands aresubstituted by(C_6H_5CO_2)~(-1)in the substitution reaction,thus producing the newtitle cluster compound,the structure of which contains two species of bidentateligand.     

MOLYBDENUM-IRON MIXED METAL CLUSTERS (Ⅰ)——THE SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF (η~5-C_5H_5)_2Mo_2Fe_2(μ_4-Te)(μ_3-Te)_2(CO)_6

The reaction of Fe_2(μ_3-Te)_2(CO)_9 with Mo_2(CO)_6(η~5-C_5H_5) affords the title compound. Its X-ray analysis shows a butterfly structure for the Mo_2Fe_2 core; the two molybdenum atoms occupy the hinge with a Mo—Mo bond distance of 2.819 and the two iron atoms are on the tops of the wings with an average Mo—Fe bond distance of 2.932(2). Each molybdenum is bonded to a Cp ring, and three CO ligands are terminally bonded to each iron atom. One tellurium atom quadruply bridges Mo_Fe_2 with Mo—Te(μ_4)=2.625(2). and Fe—Te(μ_4)=2.713(2). Two tellurium atoms triply bridge the two triangular Mo_2Fe faces with Mo—Te(μ_3)=2.678(1) and Fe—Te(μ_3)=2.513(3). The molecule has C_(2v) symmetry and a bicapped triangle bipyramidal skeleton. Crystallographic parameters are as follows: space groupImm2(orthorhombic), a=14.562(3), b=10.391(1), c=7.139(4), V=1080.2(i)~3, Z=2, ρ(cald)=1.819g·cm~(-3). The final R factor was 2.2％ for 620 independent reflections(I>2σ(I)).     

RESEARCH ON TRINUCLEAR MOLYBDENUM CLUSTER COMPOUNDS——CRYSTAL AND MOLECULAR STRUCTURE OF (C_5H_7S_2)_3[Mo_3(μ_3-S)(μ_2-S_2)_3Cl_7]

The space group of the title crystal is Pnam. The unit cell parameters are: a=17.226(4), b=14.306(7), c=15.074(4); z=4, Dobs=2.03g·cm~(-3), D_(calc)=2.063g·cm~(-3). The crystal structure was solved by the heavy atom method and refined by the full-matrix least-squares until the final conventional discrepancy factor was reduced to 0.068. The results of the investigation show that the crystal consists of trinuclear Mo cluster anions [Mo_3(μ_3-S)(μ_2-S_2)_3Cl_7]~(3-) together with planar (C_5H_7S_2)~ monocations, surrounding the cluster anions. In the cluster anion three Mo atoms, forming a nearly equilateral triangle (2.755(1), 2.755(1), 2.743(1)), are bound by a μ_3-S bridging atom, while each pair of Mo atoms is bridged further by a μ_2-S_2 ligand. Besides, each Mo atom is coordinated to two terminal Cl atoms, so that the coordination sphere of each Mo atom approaches closely a pentagonal bipyramid. In addition, a single Gl atom, not at all involved in the coordination spheres of the three Mo atom