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Volumn , Issue 9, 2007, Pages 1251-1260

N-(aryl)picolinamide complexes of ruthenium: Usual coordination and strategic cyclometalation

Author keywords

Cyclometalation; Picolinamide ligands; Ruthenium complexes

Indexed keywords

ACTIVATION ANALYSIS; AMIDES; CHLORINE COMPOUNDS; CYCLIC VOLTAMMETRY; HYDRIDES; INDIUM COMPOUNDS; ISOMERS; NAPHTHALENE; ORGANOMETALLICS; RUTHENIUM COMPOUNDS; X RAY CRYSTALLOGRAPHY;

EID: 34250790132     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200600964     Document Type: Article
Times cited : (43)

References (101)
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    • The evolved hydrogen could not be detected experimentally
    • The evolved hydrogen could not be detected experimentally.
  • 91
    • 85163240083 scopus 로고    scopus 로고
    • C. Mealli, D. M. Proserpio, CACAO Version 4.0, Italy, 1994;
    • a) C. Mealli, D. M. Proserpio, CACAO Version 4.0, Italy, 1994;
  • 93
    • 85163238876 scopus 로고    scopus 로고
    • 3 complex has little less contribution from ruthenium.
    • 3 complex has little less contribution from ruthenium.
  • 94
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    • A little dichloromethane was necessary to take the complex into solution. Addition of large excess of acetonitrile was necessary to record the redox responses in proper shape
    • A little dichloromethane was necessary to take the complex into solution. Addition of large excess of acetonitrile was necessary to record the redox responses in proper shape.
  • 98
    • 0004158053 scopus 로고
    • Experimental Electrochemistry for Chemists
    • a) D. T. Sawyer, J. L. Roberts Jr, Experimental Electrochemistry for Chemists, Wiley, New York, 1974, pp. 167-215;
    • (1974) Wiley, New York , pp. 167-215
    • Sawyer, D.T.1    Roberts Jr, J.L.2
  • 100
    • 85163237120 scopus 로고    scopus 로고
    • Chemical shifts are given in ppm and multiplicity of the signals along with the associated coupling constants (J in Hz) are given in parentheses. Overlapping signals are marked with an asterisk
    • Chemical shifts are given in ppm and multiplicity of the signals along with the associated coupling constants (J in Hz) are given in parentheses. Overlapping signals are marked with an asterisk.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.