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- [1] Reactions of the multiply-bonded dirhenium(II) complexes Re(2)X(4)(mu-dppm)(2)(CNR) (X=Cl or Br; R=t-Bu or xylyl) with alkynes. Structural characterization of [Re2Cl3(mu-dppm)(2)(CN-t-Bu)(eta(2)-HCCH)]O3SCF3 and a comparison with the related carbonyl species((1)) TRANSITION METAL CHEMISTRY, 1995, 20 (06) : 625 - 629
- [2] REACTIONS OF THE DIRHENIUM(II) COMPLEXES RE2X4(DPPM)2(X = CL OR BR DPPM = PH2PCH2PPH2) WITH ISOCYANIDES .4. ISOMERISM IN MIXED CARBONYL-ISOCYANIDE COMPLEXES OF STOICHIOMETRY [RE2CL3(DPPM)2(CO)2(CNR)]N+(N = 0 OR 1) AND [RE2CL3(DPPM)2(CO)(CNR)2]+(R = T-BU OR XYLYL), WHICH POSESS EDGE-SHARED BIOCTAHEDRAL STRUCTURESN INORGANIC CHEMISTRY, 1987, 26 (16) : 2717 - 2725
- [3] REACTIONS OF THE DICARBONYL COMPLEXES RE2X4(DPPM)2(CO)2 (X = CL, BR) AND THE MIXED CARBONYL ISOCYANIDE COMPLEXES RE2CL4(DPPM)2(CO)(CNR) (R = T-BU, XYLYL) WITH TRIMETHYLPHOSPHINE AND TRIALKYL PHOSPHITE LIGANDS - STRUCTURAL CHARACTERIZATION OF THE COMPLEXES [RE2CL3(MU-DPPM)2(CO)2L]PF6 (L = PME3, P(OET)3) THAT CONTAIN AN UNSYMMETRICAL CARBONYL BRIDGE INORGANIC CHEMISTRY, 1990, 29 (03) : 457 - 462
- [4] REACTIONS OF THE DIRHENIUM(II) COMPLEXES RE2X4(DPPM)2 (X = CL OR BR, DPPM = PH2PCH2PPH2) WITH TERTIARY PHOSPHINE AND PHOSPHITE LIGANDS - THE ISOLATION AND CHARACTERIZATION OF THE 1-1 ADDUCTS RE2X4(DPPM)2(PR3) AND RE2CL4(DPPM)2[P(OR)3] AND THE CRYSTAL-STRUCTURE OF [RE2CL3(DPPM)2(NCET)2]PF6 INORGANICA CHIMICA ACTA, 1990, 172 (01) : 65 - 71
- [5] REACTIONS OF THE DIRHENIUM(II) COMPLEXES RE2X4(DPPM)2 (X = CL, BR - DPPM = PH2PCH2PPH2) WITH ISOCYANIDES .5. MIXED CARBONYL ISOCYANIDE AND CARBONYL ISOCYANIDE NITRILE COMPLEXES OF STOICHIOMETRY [RE2CL3(DPPM)2(CO)(CNR)(L)]PF6 (R = TERT-BU, XYL (XYLYL) - L = TERT-BUNC, XYLNC, MECN, ETCN) - STRUCTURAL CHARACTERIZATION OF THE CATION [CL2(CO)RE(MU-DPPM)2RECL(CN-TERT-BU)2]+L INORGANIC CHEMISTRY, 1988, 27 (15) : 2601 - 2607
- [6] Reactions of the dirhenium(II) complexes Re2X4(μ-dppm)2 (X = Cl, Br; dppm = Ph2PCH2PPh2) with isocyanides.: 19.: Studies of the reactions of five structural isomers of Re2Cl2(μ-dppm)2(CO)(CNXyl)3 that lead to the dirhenium(I) complexes [Re2(μ-Cl)(μ-CO)(μ-dppm)2(CNXyl)4]O3SCF3 and [Re2Cl(μ-dppm)2(CO)(CNXyl)3(NCCH3)]O3SCF3 INORGANIC CHEMISTRY, 1999, 38 (22) : 5165 - 5170
- [7] Reactions of the dirhenium(II) complexes Re2X4(μ-dppm)2 (X = Cl, Br;: dppm = Ph2PCH2PPh2) with isocyanides.: 21.1: A comparison with the complexes Re2Cl4(μ-dppE)2 and Re2Cl4(μ-dcpm)2 (dppE = Ph2PC(=CH2)PPh2;: dcpm = Cy2PCH2PCy2) and the structural characterization of complexes of the types Re2Cl4(μ-LL)2(CNR), Re2Cl4(μ-LL)2(CNR)2, and [Re2Cl3(μ-LL)2(CNR)3]+ (LL = dppm, dppE, dcpm;: R = t-Bu, Xyl) INORGANIC CHEMISTRY, 2000, 39 (12) : 2676 - 2683
- [8] Reactions of the dirhenium(II) complexes Re2X4(μ-dppm)2 (X = Cl, Br;: dppm = Ph2PCH2PPh2) with isocyanides.: Part XVII.: Isomerizations of triply bonded dirhenium complexes of the type [Re2X3(μ-dppm)2(CO)(CNXyl) (CNR)]+ (R = Xyl or t-Bu) with open bioctahedral structures to di-μ-chloro edge-sharing bioctahedral structures with no Re-Re bond JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1999, 573 (1-2) : 87 - 95