The observed magnetic data for two isosceles tricobalt(II) complexes have been successfully analyzed, considering the axial distortion around each cobalt(II) ion, the local spin-orbit coupling, the anisotropic exchang...The observed magnetic data for two isosceles tricobalt(II) complexes have been successfully analyzed, considering the axial distortion around each cobalt(II) ion, the local spin-orbit coupling, the anisotropic exchange interactions, and the intermolecular exchange interactions. The complexes each contains two types of octahedral high-spin cobalt(II) ions (CoA and CoB) in the shape of an isosceles triangle (CoA1–CoB–CoA2), and the contribution of the orbital angular momentum is significant. The exchange interaction between the CoA and CoB ions is practically negligible (J = ~ 0), whereas the interaction between the CoA1 and CoA2 ions is ferromagnetic (J’ > 0) for both complexes.展开更多
Compound Co_3(o-HOC_6H_4S)_2(o-OC_6H_4S)_2(PEt_3)_3 was obtained by reaction of CoCl_2, o-HOC_6H_4SH(H_2mD)and PEt_3 in ethanol in the presence of NaOCH_3.The three Co atoms are triangularly arranged and asymmetricall...Compound Co_3(o-HOC_6H_4S)_2(o-OC_6H_4S)_2(PEt_3)_3 was obtained by reaction of CoCl_2, o-HOC_6H_4SH(H_2mD)and PEt_3 in ethanol in the presence of NaOCH_3.The three Co atoms are triangularly arranged and asymmetrically bridged by four S and one O atoms from the four H_2mp ligands and terminally ligated by one O and three P atoms.Two free hydroxyl groups form two internal hydrogen bonds with adjacent oxo donor atoms.展开更多
CH_3CCo_3(CO)_9 was synthesized from the reaction between chloralose and Co_2(CO)_. The radical anion was generated by electrochemical reduction,and electron spin resonance spectra in THF were recorded by in situ elec...CH_3CCo_3(CO)_9 was synthesized from the reaction between chloralose and Co_2(CO)_. The radical anion was generated by electrochemical reduction,and electron spin resonance spectra in THF were recorded by in situ electrolysis in the sample tube in the ESR cavity at 298 and 110K with the spectral data展开更多
By the reaction of Co2(CO)8 with 2-thiohydantoins S-CNHC(O)C(R1) (R2)NC(O)R3(HL), a new cluster with formula Co3(CO)7 (μ3-S) (μ3, η2-S CNC(O)C(CH3)2N C(O)CH3 hasbeen prepared. The cluster has been characterized by ...By the reaction of Co2(CO)8 with 2-thiohydantoins S-CNHC(O)C(R1) (R2)NC(O)R3(HL), a new cluster with formula Co3(CO)7 (μ3-S) (μ3, η2-S CNC(O)C(CH3)2N C(O)CH3 hasbeen prepared. The cluster has been characterized by elemental analysis, IR, 1H NMR and MS spectroscopy.The crystal structure of the cluster has been determined by X-ray single crystal diffraction method.The crystal of the cluster is triclinic, belonging to space group P1 and the cell parameters are as follows: a=8.456 (3), b=11.534(3), c= l1.990(4)A, α=107.36(3), β=108.44(5), γ=90.,18(3)°. Thestructural analysis shows that this molecule contains a tetrahedral cluster framword Co3S and2-thiohydantoin as bridging ligands links up with two cobalt atoms of the framwork by S- andN-atom thus -a five member ring of Co2 NCS has been formed.展开更多
Eight metal cluster compounds have been synthesized from parent compound （μ3-CPh）Co3-（CO）9 and triphenylphosphine（arsine,stibine,bismuthine）. All the compounds were characterized by elemental analysis and IR sp...Eight metal cluster compounds have been synthesized from parent compound （μ3-CPh）Co3-（CO）9 and triphenylphosphine（arsine,stibine,bismuthine）. All the compounds were characterized by elemental analysis and IR spectrometry. They results showed that their catalytic activities for 1-butene hydroformylation and the yields of product both were higher than that of the parent compound in 97% and 20% more, respectively, at reaction conditions of 303.5 K, 0.392 MPa, and for 48 hours. The catalytic activities and the ratio of nor to iso by using PhCCo3（CO）7（APh3）m were increased with increase in the atomic numbers of element A（A=P,As,Sb,Bi）.展开更多
文摘The observed magnetic data for two isosceles tricobalt(II) complexes have been successfully analyzed, considering the axial distortion around each cobalt(II) ion, the local spin-orbit coupling, the anisotropic exchange interactions, and the intermolecular exchange interactions. The complexes each contains two types of octahedral high-spin cobalt(II) ions (CoA and CoB) in the shape of an isosceles triangle (CoA1–CoB–CoA2), and the contribution of the orbital angular momentum is significant. The exchange interaction between the CoA and CoB ions is practically negligible (J = ~ 0), whereas the interaction between the CoA1 and CoA2 ions is ferromagnetic (J’ > 0) for both complexes.
文摘Compound Co_3(o-HOC_6H_4S)_2(o-OC_6H_4S)_2(PEt_3)_3 was obtained by reaction of CoCl_2, o-HOC_6H_4SH(H_2mD)and PEt_3 in ethanol in the presence of NaOCH_3.The three Co atoms are triangularly arranged and asymmetrically bridged by four S and one O atoms from the four H_2mp ligands and terminally ligated by one O and three P atoms.Two free hydroxyl groups form two internal hydrogen bonds with adjacent oxo donor atoms.
文摘CH_3CCo_3(CO)_9 was synthesized from the reaction between chloralose and Co_2(CO)_. The radical anion was generated by electrochemical reduction,and electron spin resonance spectra in THF were recorded by in situ electrolysis in the sample tube in the ESR cavity at 298 and 110K with the spectral data
文摘By the reaction of Co2(CO)8 with 2-thiohydantoins S-CNHC(O)C(R1) (R2)NC(O)R3(HL), a new cluster with formula Co3(CO)7 (μ3-S) (μ3, η2-S CNC(O)C(CH3)2N C(O)CH3 hasbeen prepared. The cluster has been characterized by elemental analysis, IR, 1H NMR and MS spectroscopy.The crystal structure of the cluster has been determined by X-ray single crystal diffraction method.The crystal of the cluster is triclinic, belonging to space group P1 and the cell parameters are as follows: a=8.456 (3), b=11.534(3), c= l1.990(4)A, α=107.36(3), β=108.44(5), γ=90.,18(3)°. Thestructural analysis shows that this molecule contains a tetrahedral cluster framword Co3S and2-thiohydantoin as bridging ligands links up with two cobalt atoms of the framwork by S- andN-atom thus -a five member ring of Co2 NCS has been formed.
文摘Eight metal cluster compounds have been synthesized from parent compound （μ3-CPh）Co3-（CO）9 and triphenylphosphine（arsine,stibine,bismuthine）. All the compounds were characterized by elemental analysis and IR spectrometry. They results showed that their catalytic activities for 1-butene hydroformylation and the yields of product both were higher than that of the parent compound in 97% and 20% more, respectively, at reaction conditions of 303.5 K, 0.392 MPa, and for 48 hours. The catalytic activities and the ratio of nor to iso by using PhCCo3（CO）7（APh3）m were increased with increase in the atomic numbers of element A（A=P,As,Sb,Bi）.
