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  • 1
    ISSN: 0009-2940
    Keywords: Macrocyclic (alkene dithiolato)mercury complexes ; Dithiolato complexes ; Stilbene-α,β1-dithiol complexes ; Mercury(II) macrocyclic dithiolato complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of the ligand cis - -S—C(Ph)≡C(Ph)-S-[CH2]n - S - C(Ph)=C(Ph)-S- with n=3 (dianion of 1) with HgCl2 in ethanol produces a yellow linearly trinuclear, μ1-S and μ1-Cl-bridged complex of composition C62H52Cl2Hg3S8 (4), in which the central Hg(II) ion is in a near octahedral arrangement of four Hg—S and two Hg—Cl bonds, whereas the two terminal Hg(II) ions are tetracoordinated with three Hg—S bonds and one Hg—Cl bond in distorted tetrahedral arrangements. The two ligands are bidentate with respect to the terminal and central Hg(II) ions. The corresponding ligand with n=4 (dianion of 2) reacts with HgCl2 to yield a yellow Hg(II) complex of composition C32H28HgS4 (5), in which the ligand is tetradentate and in the trans-syn configuration. The Hg(II) ion in the unit cell of 5 is pentacoordinated, due to symmetric dimerization of two molecules of 2 by two weak coordinate Hg—S bonds of 3.442(2) Å length.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1355-1357 
    ISSN: 0009-2940
    Keywords: Diphosphanylhydrazides ; Diphosphanes, dinitrogen-bridged ; Cycloplatinaphosphahydrazides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: While the transition metal complexes of bis(phosphanyl)amines (PII-N-PIII) have been known for over three decades, the ligating properties of the next homologue PIII-N-N-PIII have been unprecedented so far. The X-ray structures of cycloplatinaphosphanehydrazides, [(OR)2PN(Me)N(Me)P(OR)2-PtCl2], reveal short distances for the P-N [1.639(5) Å] bonds.
    Additional Material: 2 Ill.
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  • 3
    ISSN: 0009-2940
    Keywords: Cyclophosphahydrazides ; Dinitrogen-bridged ; Conformation ; Chair and Boat forms ; Dinuclear Mo(0) complexes ; 1,2,4,5,3,6-Tetrazadiphosphorinanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of methylhydrazine with RPC12 (R = Et, tBu, and Ph) produced the cyclic phosphorus (III) hydrazides (1,2,4,5,3,6-tetrazadiphosphorinanes) [RPN(Me)N(H)2 (R = Et, 1; (Ph, 2; tBu, 3) in good yields. The 1H-and 31P-NMR spectroscopic analysis indicated that 1 exists in chair and boat conformations. However, it crystallizes in the chair conformation exclusively. The X-ray crystallographic investigation of all the three cyclo-phosphorus hydrazides 1-3 confirms the existence of these compounds in the chair conformations in the solid state. The reaction of Mo(CO)4-(NHC5H10)2 with 1 and 2 gives the dinuclear Mo(0) complexes [{Mo(CO)4(NHC5H10)}2(μ-[RPN(Me)N(H)]2}] (R = Et, 5; Ph, 6). Based on 1H- and 31P-NMR spectroscopic data, a bridging dinuclear dimetallic formulation is proposed for 5 and 6. The IR spectra indicate that the carbonyls are disposed in cis-geometry around the Mo(0) center.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2367-2371 
    ISSN: 0009-2940
    Keywords: Tin, (alkylthio)stilbene complexes of ; cis-stilbene-α-thiol, β-(methylthio)-, tin(IV) complexes of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The S-methyl-cis-stilbene-α,β-dithiolate of Sn(IV), Sn[Ph(S)C=C(SCH3)Ph]4, has an octacoordinate structure with two sets of four covalent and coordinate Sn-S and Sn-S(CH3) bonds of 2.425(3) and 3.599(3) Å, respectively. Both types of Sn-S bonds are close to being tetrahedral, the coordination geometry is a distorted cube. This unprecedented structure appears to involve conventional covalent and outer-sphere coordinative Sn-S bonds. In the diphenyl derivative Ph2Sn[Ph(S)C=C(SCH3)Ph]2 the SnC2S2 core formed by the covalent Sn-C and Sn-S(thiolato) bonds is tetrahedral, but two coordinate outer-sphere Sn-S(CH3) bonds of 3.500(3) Å are also present. In the related SnCl2[Ph(S)C=C(SCH3)Ph]2 the presence of the polar Sn-Cl bonds prevents outer-sphere bonding; the coordination geometry is distorted octahedral. In the triphenyltin derivative Ph3Sn[Ph(S)C=C(SCH3)Ph] the coordination geometry is tetrahedral, the thiol-thioether ligand being monodentate with the SCH3 group in a non-interactive position.
    Additional Material: 5 Ill.
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