Reactions of linked tetrahedron clusters [Co2(CO)6(μ-HC2CH2O)–]2R with Rh2(CO)4Cl2 to give mixed-metal linked alkyne-bridged butterfly clusters containing C2Co2Rh2 unit
摘要:
The reactions of compound Rh-2(CO)(4)Cl-2, 1 with [Co-2(CO)(6)(mu-HC2CH2O)-](2)R (R = C6H4, 2; (COCH2)(2), 3; C6H4-1,4-(CO)(2), 4; (COCH)(2), 5; (CO)(2), 6) in benzene at 60 degrees C produce five new mixed-metal linked clusters Rh2CO2(CO)(10)(mu(4),eta(2) -HC2CH2O-R-OCH2C2H-mu) OCH2C2H-mu) (R = C6H4, 7a; (COCH2)(2), 7b; C6H4-1,4-(CO)(2), 7c; (COCH)(2), 7d; (CO)2, 7e) and five known linked octahedral clusters [Rh2Co2)(CO)(10)(mu(4)eta(2)-HC2CH2O-)](2)R (R = C6H4, 8a; (COCH2)(2), 8b; C6H4-1,4-(CO)(2), 8c; (COCH)(2), 8d; (CO)(2), 8e), respectively. Treatment of clusters 7a-8e in benzene at room temperature under air for 24 h with stirring afford the precursor clusters 2-6, respectively. The structure of cluster 7a has been determined by single-crystal X-ray diffraction. The linked cluster 7a possesses two isomers A and B in its structures, the Rh-2(CO)(4) unit inserts into one of two Co-Co bonds and coordinates to the Co2C2 core forming one distorted closo-Rh2CO2C2 octahedron framework which is connected to the Co2C2 tetrahedron unit via C6H4(OCH2)(2)-1,4 as a bridging ligand. All clusters were characterized by C, H elemental analysis, IR and H-1 NMR spectroscopy. (c) 2005 Published by Elsevier B.V.
DOI:
10.1016/j.jorganchem.2005.09.014
作为产物:
描述:
[Rh2Co2(CO)10(μ4,η2-HC2CH2OC6H4-1,4-(CO)2-OCH2C2H-μ)Co2(CO)6] 在
air 作用下,
以
苯 为溶剂,
以40.6%的产率得到[(Co2(CO)6(μ4,η2-HC2CH2O))2C6H4-1,4(CO)2]
参考文献:
名称:
Reactions of linked tetrahedron clusters [Co2(CO)6(μ-HC2CH2O)–]2R with Rh2(CO)4Cl2 to give mixed-metal linked alkyne-bridged butterfly clusters containing C2Co2Rh2 unit
摘要:
The reactions of compound Rh-2(CO)(4)Cl-2, 1 with [Co-2(CO)(6)(mu-HC2CH2O)-](2)R (R = C6H4, 2; (COCH2)(2), 3; C6H4-1,4-(CO)(2), 4; (COCH)(2), 5; (CO)(2), 6) in benzene at 60 degrees C produce five new mixed-metal linked clusters Rh2CO2(CO)(10)(mu(4),eta(2) -HC2CH2O-R-OCH2C2H-mu) OCH2C2H-mu) (R = C6H4, 7a; (COCH2)(2), 7b; C6H4-1,4-(CO)(2), 7c; (COCH)(2), 7d; (CO)2, 7e) and five known linked octahedral clusters [Rh2Co2)(CO)(10)(mu(4)eta(2)-HC2CH2O-)](2)R (R = C6H4, 8a; (COCH2)(2), 8b; C6H4-1,4-(CO)(2), 8c; (COCH)(2), 8d; (CO)(2), 8e), respectively. Treatment of clusters 7a-8e in benzene at room temperature under air for 24 h with stirring afford the precursor clusters 2-6, respectively. The structure of cluster 7a has been determined by single-crystal X-ray diffraction. The linked cluster 7a possesses two isomers A and B in its structures, the Rh-2(CO)(4) unit inserts into one of two Co-Co bonds and coordinates to the Co2C2 core forming one distorted closo-Rh2CO2C2 octahedron framework which is connected to the Co2C2 tetrahedron unit via C6H4(OCH2)(2)-1,4 as a bridging ligand. All clusters were characterized by C, H elemental analysis, IR and H-1 NMR spectroscopy. (c) 2005 Published by Elsevier B.V.
Reactions of dipropargyl manolate, terephthalate with Co2(CO)8, Mo2Cp2(CO)4 and RuCo2(CO)11 give the di or tetranuclear clusters. The crystal structure of [CH2(CO2CH2C2H-μ)2][Co2(CO)6]2 and [p-(HC2CH2OCO)C6H4(CO2CH2C2H-μ)][Co2(CO)6]
dipropargyl manolate and terephthalate, respectively, with Co2(CO)8 in THF at room temperature gave four new compounds [R(CO2CH2C2H-μ)2][Co2(CO)6]2 (R=CH2, 1a; R=C6H4, 1b) and [(HC2CH2OCO)R(CO2CH2C2H-μ)][Co2(CO)6] (R=CH2, 2a; R=C6H4-1,4-, 2b), and compounds 2a and b reacted with RuCo2(CO)11 to form two new linked clusters [R(CO2CH2C2H-μ)2][Co2(CO)6][RuCo2(CO)9] (R=CH2, 3a; R=C6H4-1,4-, 3b). The treatment of
摘要室温下,二炔丙基马来酸酯和对苯二甲酸酯与Co2(CO)8在THF中的反应在室温下产生了四个新化合物[R(CO2 C2H-μ)2] [Co2(CO)6] 2(R = CH2,1a; R = C6H4,1b)和[(HC2 OCO)R(CO2 C2H-μ)] [Co2(CO)6](R = ,2a; R = -1,4-,2b),化合物2a和b反应与RuCo2(CO)11形成两个新的链接簇[R(CO2 C2H-μ)2] [Co2(CO)6] [RuCo2(CO)9](R = ,3a; R = -1,4- ,3b)。分别用RuCo2(CO)11处理两种二炔丙基酯可得到另外两个新簇[R(CO2 C2H-μ)2] [RuCo2(CO)9] 2(R = ,4a; R = -1, 4-,4b)。马来酸二炔丙基酯,对苯二甲酸酯与Mo2Cp2(CO
PREPARATION AND CHARACTERIZATION OF SOME DIMERIC η<sup>2</sup>-DIYNE COMPLEXES OF COBALT
作者:Yu-Hua Zhang、Zhi Chen、Wei-Qiang Zhang、Yuan-Qi Yin、Zhong-Yuan Zhou、Albert S. C. Chan
DOI:10.1081/sim-120005618
日期:2002.11.7
The organometallic dimers, [R(CO2CH2C2H-mu)(2)}CO2(CO)(6)}(2)] [R = C6H4-1,4 (1), (CH)(2) (2), (CH2)(2) (3)], have been prepared from reactions between CO2(CO)(8) and appropriate diyne ligands in tetrahydrofuran at room temperature. These complexes have been characterized by IR spectra, H-1 NMR spectra and elemental analyses. The structure of (1) was determined by single crystal X-ray diffraction. The compound (1), C26H10O16Co4, Mr = 814.06, is triclinic, space group P (1) over bar, with unit cell dimensions a = 8.139(2), b 8.803(3), c = 11.343(3) Angstrom, alpha = 99.421(6), beta = 96.260(6), gamma = 102.772(6)degrees. The cobalt atom is coordinated by three terminal carbon is and an alkynyl group. The Co-Co bond length is 2.4834(7) Angstrom.