Transition metal complexes containing all-carbon ligands

[41] Higher nuclearity Fe,Ru mixed-metal dicarbide cluster compounds derived from ethynediyldiiron complex (η5-C5Me5)(CO)2Fe-CC-Fe(η5-C5Me5)(CO)2 [J]. ORGANOMETALLICS, 2001, 20 (08) : 1555 - 1568

[42] REACTION OF THE CATIONIC DIIRON MU-ETA-1-ETA-2-ACETYLIDE COMPLEXES [(FP)2(C=CR)]BF4 (R = H, PH) WITH NAOME [J]. ORGANOMETALLICS, 1991, 10 (05) : 1561 - 1568

[43] STRUCTURE AND REACTIVITY OF C2 SPECIES ON POLYMETALLIC SYSTEMS [J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1995, 68 (02) : 420 - 432

[44] PREPARATION, STRUCTURE, AND DIVERGENT FLUXIONAL BEHAVIOR OF CATIONIC DINUCLEAR IRON ACETYLIDES [FPSTAR2(C=C-H)]BF4, [FPSTAR2(C=C-PH)]BF4 [J]. ORGANOMETALLICS, 1990, 9 (03) : 816 - 825

[45] INTERACTION OF IRON ETHYNYL AND ETHYNEDIYL COMPLEXES WITH CP2NI2(CO)2 - FORMATION OF TRINUCLEAR AND TETRANUCLEAR ADDUCTS WITH A MULTIPLY BRIDGING C2H LIGAND [J]. ORGANOMETALLICS, 1992, 11 (10) : 3468 - 3472

[46] Formation of novel conjugated polycarbon-metal systems via metal migration on a M-CC-CC-M linkage [J]. CHEMICAL COMMUNICATIONS, 2000, (14) : 1285 - 1286

[47] Reaction of ethynediyl, butadiynediyl and ethynyl iron complexes, (η5-C5R5)(CO)2Fe-(CC)n-X [X = Fe(η5-C5R5)(CO)2, H;: R5 = Me5, Me4Et; n = 1, 2], with Fe2(CO)9 leading to polynuclear C2 and C4 complexes [J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1998, 565 (1-2) : 49 - 62

[48] Facile CC bond cleavage of polyynediyldiiron complexes, Fp*-(CC)n-Fp* [Fp*=Fe(η5-C5Me5)(CO)2, n = 3, 4], with Fe2(CO)9 leading to bis(μ3-alkylidyne) complexes, Fp*-CC-μ3-C-Fe3(CO)9-μ3-C-(CC)n-2-Fp* [J]. CHEMICAL COMMUNICATIONS, 1999, (01) : 101 - 102

[49] INTERACTION OF ETHYNYLIRON (FP-C-EQUIVALENT-TO-C-H AND FP-ASTERISK-C-EQUIVALENT-TO-C-H) AND ETHYNEDIYLDIIRON COMPLEXES (FP-ASTERISK-C-EQUIVALENT-TO-C-FP-ASTERISK) WITH CO2(CO)8 - FORMATION OF A CLUSTER COMPOUND WHICH IS FLUXIONAL VIA A METAL METAL BOND SCISSION AND RECOMBINATION PROCESS [J]. ORGANOMETALLICS, 1992, 11 (05) : 1825 - 1830

[50] AKITA M, 2002, CHEM COMMUN, P1284

[41] Higher nuclearity Fe,Ru mixed-metal dicarbide cluster compounds derived from ethynediyldiiron complex (η5-C5Me5)(CO)2Fe-CC-Fe(η5-C5Me5)(CO)2 [J]. ORGANOMETALLICS, 2001, 20 (08) : 1555 - 1568

[42] REACTION OF THE CATIONIC DIIRON MU-ETA-1-ETA-2-ACETYLIDE COMPLEXES [(FP)2(C=CR)]BF4 (R = H, PH) WITH NAOME [J]. ORGANOMETALLICS, 1991, 10 (05) : 1561 - 1568

[43] STRUCTURE AND REACTIVITY OF C2 SPECIES ON POLYMETALLIC SYSTEMS [J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1995, 68 (02) : 420 - 432

[44] PREPARATION, STRUCTURE, AND DIVERGENT FLUXIONAL BEHAVIOR OF CATIONIC DINUCLEAR IRON ACETYLIDES [FPSTAR2(C=C-H)]BF4, [FPSTAR2(C=C-PH)]BF4 [J]. ORGANOMETALLICS, 1990, 9 (03) : 816 - 825

[45] INTERACTION OF IRON ETHYNYL AND ETHYNEDIYL COMPLEXES WITH CP2NI2(CO)2 - FORMATION OF TRINUCLEAR AND TETRANUCLEAR ADDUCTS WITH A MULTIPLY BRIDGING C2H LIGAND [J]. ORGANOMETALLICS, 1992, 11 (10) : 3468 - 3472

[46] Formation of novel conjugated polycarbon-metal systems via metal migration on a M-CC-CC-M linkage [J]. CHEMICAL COMMUNICATIONS, 2000, (14) : 1285 - 1286

[47] Reaction of ethynediyl, butadiynediyl and ethynyl iron complexes, (η5-C5R5)(CO)2Fe-(CC)n-X [X = Fe(η5-C5R5)(CO)2, H;: R5 = Me5, Me4Et; n = 1, 2], with Fe2(CO)9 leading to polynuclear C2 and C4 complexes [J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1998, 565 (1-2) : 49 - 62

[48] Facile CC bond cleavage of polyynediyldiiron complexes, Fp*-(CC)n-Fp* [Fp*=Fe(η5-C5Me5)(CO)2, n = 3, 4], with Fe2(CO)9 leading to bis(μ3-alkylidyne) complexes, Fp*-CC-μ3-C-Fe3(CO)9-μ3-C-(CC)n-2-Fp* [J]. CHEMICAL COMMUNICATIONS, 1999, (01) : 101 - 102

[49] INTERACTION OF ETHYNYLIRON (FP-C-EQUIVALENT-TO-C-H AND FP-ASTERISK-C-EQUIVALENT-TO-C-H) AND ETHYNEDIYLDIIRON COMPLEXES (FP-ASTERISK-C-EQUIVALENT-TO-C-FP-ASTERISK) WITH CO2(CO)8 - FORMATION OF A CLUSTER COMPOUND WHICH IS FLUXIONAL VIA A METAL METAL BOND SCISSION AND RECOMBINATION PROCESS [J]. ORGANOMETALLICS, 1992, 11 (05) : 1825 - 1830

[50] AKITA M, 2002, CHEM COMMUN, P1284