A new ruthenium（II） complex with two different types oftridentate ligands was synthesized, 2,2′：6′,2″-terpyridine （tpy） and 2,6-Bis（（N-benzyl）aminomethyl）pyridine （bbap）： [Ru（tpy）（bbap）]2＋ （1）. T...A new ruthenium（II） complex with two different types oftridentate ligands was synthesized, 2,2′：6′,2″-terpyridine （tpy） and 2,6-Bis（（N-benzyl）aminomethyl）pyridine （bbap）： [Ru（tpy）（bbap）]2＋ （1）. This compound was designed to form intramolecular π-π stacking interaction between tpy and substituted benzyl groups of bbap. The single-crystal X-ray diffraction analysis revealed that 1 crystallized with orthorhombic space group Aea2 and the ruthenium center has a distorted octahedral coordination geometry with fully chelated tpy and bbap ligands. Simultaneously, in the crystal structure of 1, the central part of ligating tpy was stacked and sandwiched with a pair of capped benzyl substituent groups of bbap, the nearest atomic distance being N...C = 3.28 A.展开更多
Three stable 4-substituted pyridine-based ruthenium（II）complexes[RuCl2（PPh3）L]（L=4-R-2,6-bis （diethylaminomethylene）pyridine,R=Br,H or allyloxy）were synthesized.The catalytic activities of the complexes toward...Three stable 4-substituted pyridine-based ruthenium（II）complexes[RuCl2（PPh3）L]（L=4-R-2,6-bis （diethylaminomethylene）pyridine,R=Br,H or allyloxy）were synthesized.The catalytic activities of the complexes toward transfer hydrogenation from alcohols to ketones were investigated.The electronic effects of the para-substituent in the pyridyl ring were probed and we found that the electron-donating group increased the catalytic activity.The result suggests that an electron-donating group is probably preferential for linking the catalytic ruthenium complex and the chemically inert supporting molecules such as a carbosilane dendrimer.展开更多
The synthesis and characterization of several hexa – coordinated Ru(II) complexes of the type [Ru(CO)(B)(L)] (B = PPh3/AsPh3/py/pip;L = di-basic tetradentate ligand derived from the condensation of isatin with diamin...The synthesis and characterization of several hexa – coordinated Ru(II) complexes of the type [Ru(CO)(B)(L)] (B = PPh3/AsPh3/py/pip;L = di-basic tetradentate ligand derived from the condensation of isatin with diamines) were reported. IR, electronic, 1H- NMR, 31P-NMR of the complexes are discussed. An octahedral geometry has been tentatively proposed for all these complexes. The new complexes have been tested for the catalytic activity in the reaction of oxidation of alcohols in the presence of N-me- thylmorpholine–N-oxide as co-oxidant. The new complexes were also exhibited antimicrobial investigations.展开更多
Four novel mononuclear ruthenium(II) complexes [Ru-(dmb) 2L] 2+ [dmb=4,4′-dimethyl-2,2′-bipyridine, L=imid-azo-[4,5-f]phenanthroline (IP), 2-phenylimidazo-phenanthroline (PIP), 2-(4′-hydroxyphenyl)imidazo-phe...Four novel mononuclear ruthenium(II) complexes [Ru-(dmb) 2L] 2+ [dmb=4,4′-dimethyl-2,2′-bipyridine, L=imid-azo-[4,5-f]phenanthroline (IP), 2-phenylimidazo-phenanthroline (PIP), 2-(4′-hydroxyphenyl)imidazo-phenanthroline (HOP), 2-(4′-dimethylami- nophenyl)imidazo-phenanthroline (DMNP)] were synthesized and characterized by ES-MS, 1H NMR, UV-vis and electrochemistry. The nonlinear optical properties of the ruthenium(II) complexes were investigated by Z-scan techniques with 12 ns laser pulse at 540 nm, and all of them exhibit both nonlinear optical (NLO) absorption and self-defocusing effect. The corresponding effective NLO susceptibility |χ 3| of the complexes is in the range of 2.68×10 -12-4.57×10 -12 esu.展开更多
Electrochemical assembly of [Ru（bpy）2dppz]^2＋{bpy=2,2＇-bipyridine, dppz=dipyrido[3,2-a：＂2＇,3＇-c]phenazine} on an ITO electrode in the presence of guanine and photoelectroehemical properties of the assembled la...Electrochemical assembly of [Ru（bpy）2dppz]^2＋{bpy=2,2＇-bipyridine, dppz=dipyrido[3,2-a：＂2＇,3＇-c]phenazine} on an ITO electrode in the presence of guanine and photoelectroehemical properties of the assembled layer were investigated. It has been found that [Ru（bpy）2dppz]^3＋/2＋ can be assembled onto the ITO electrode by the method of repetitive voltammetric sweeping, and the assembly is enhanced by guanine. The peak currents of prewaves increase linearly up to a guanine concentration of 0.25 mmol/L. More importantly, upon illumination with 470 nm light source and at an applied potential of 0.2 V, cathodic current for the fabricated layer on the ITO electrode indicate a linear enhancement with the rise of guanine concentration. Meanwhile, [Ru（bpy）2dppz]^2＋ can be served as an excellent mediator to prompt the oxidation of guanine, and the mediated peak current increases linearly with added guanine concentration from 0.01 to 0.25 mmol/L. In addition, the assembly mechanism of [Ru（bpy）2dppz]^2＋ on the ITO electrode associated with the oxidation of guanine and the assistance of light irradiation were discussed.展开更多
文摘A new ruthenium（II） complex with two different types oftridentate ligands was synthesized, 2,2′：6′,2″-terpyridine （tpy） and 2,6-Bis（（N-benzyl）aminomethyl）pyridine （bbap）： [Ru（tpy）（bbap）]2＋ （1）. This compound was designed to form intramolecular π-π stacking interaction between tpy and substituted benzyl groups of bbap. The single-crystal X-ray diffraction analysis revealed that 1 crystallized with orthorhombic space group Aea2 and the ruthenium center has a distorted octahedral coordination geometry with fully chelated tpy and bbap ligands. Simultaneously, in the crystal structure of 1, the central part of ligating tpy was stacked and sandwiched with a pair of capped benzyl substituent groups of bbap, the nearest atomic distance being N...C = 3.28 A.
基金Supported by the National Natural Science Foundation of China（20576052） the Joint Innovation Fund of Jiangsu Province（BY2009107） the National Basic Research Program of China（2003CB615707）
文摘Three stable 4-substituted pyridine-based ruthenium（II）complexes[RuCl2（PPh3）L]（L=4-R-2,6-bis （diethylaminomethylene）pyridine,R=Br,H or allyloxy）were synthesized.The catalytic activities of the complexes toward transfer hydrogenation from alcohols to ketones were investigated.The electronic effects of the para-substituent in the pyridyl ring were probed and we found that the electron-donating group increased the catalytic activity.The result suggests that an electron-donating group is probably preferential for linking the catalytic ruthenium complex and the chemically inert supporting molecules such as a carbosilane dendrimer.
文摘The synthesis and characterization of several hexa – coordinated Ru(II) complexes of the type [Ru(CO)(B)(L)] (B = PPh3/AsPh3/py/pip;L = di-basic tetradentate ligand derived from the condensation of isatin with diamines) were reported. IR, electronic, 1H- NMR, 31P-NMR of the complexes are discussed. An octahedral geometry has been tentatively proposed for all these complexes. The new complexes have been tested for the catalytic activity in the reaction of oxidation of alcohols in the presence of N-me- thylmorpholine–N-oxide as co-oxidant. The new complexes were also exhibited antimicrobial investigations.
文摘Four novel mononuclear ruthenium(II) complexes [Ru-(dmb) 2L] 2+ [dmb=4,4′-dimethyl-2,2′-bipyridine, L=imid-azo-[4,5-f]phenanthroline (IP), 2-phenylimidazo-phenanthroline (PIP), 2-(4′-hydroxyphenyl)imidazo-phenanthroline (HOP), 2-(4′-dimethylami- nophenyl)imidazo-phenanthroline (DMNP)] were synthesized and characterized by ES-MS, 1H NMR, UV-vis and electrochemistry. The nonlinear optical properties of the ruthenium(II) complexes were investigated by Z-scan techniques with 12 ns laser pulse at 540 nm, and all of them exhibit both nonlinear optical (NLO) absorption and self-defocusing effect. The corresponding effective NLO susceptibility |χ 3| of the complexes is in the range of 2.68×10 -12-4.57×10 -12 esu.
基金Supported by the Natural Science Foundation of Guangdong Province,China(Nos.2004J1-C0091 and Z03020)
文摘Electrochemical assembly of [Ru（bpy）2dppz]^2＋{bpy=2,2＇-bipyridine, dppz=dipyrido[3,2-a：＂2＇,3＇-c]phenazine} on an ITO electrode in the presence of guanine and photoelectroehemical properties of the assembled layer were investigated. It has been found that [Ru（bpy）2dppz]^3＋/2＋ can be assembled onto the ITO electrode by the method of repetitive voltammetric sweeping, and the assembly is enhanced by guanine. The peak currents of prewaves increase linearly up to a guanine concentration of 0.25 mmol/L. More importantly, upon illumination with 470 nm light source and at an applied potential of 0.2 V, cathodic current for the fabricated layer on the ITO electrode indicate a linear enhancement with the rise of guanine concentration. Meanwhile, [Ru（bpy）2dppz]^2＋ can be served as an excellent mediator to prompt the oxidation of guanine, and the mediated peak current increases linearly with added guanine concentration from 0.01 to 0.25 mmol/L. In addition, the assembly mechanism of [Ru（bpy）2dppz]^2＋ on the ITO electrode associated with the oxidation of guanine and the assistance of light irradiation were discussed.
