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Volumn 28, Issue 15, 2009, Pages 4624-4627

Formation of an iodide-bridged diruthenium complex from [(n 5-Ph4C4COH)(CO)2RuI] and [(Ph 4C4CO)(CO)2Ru]2: An efficient catalyst for alcohol oxidation with Ag2O

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL OXIDATION; CATALYTIC ACTIVITY; DIRUTHENIUM COMPLEX; EFFICIENT CATALYSTS; OXIDATION OF ALCOHOLS; ROOM TEMPERATURE; SILVER OXIDES;

EID: 68149098744     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9003434     Document Type: Article
Times cited : (26)

References (36)
  • 27
    • 68149128483 scopus 로고    scopus 로고
    • Despite the presence of an intervening octahedral calcium fragment, the Ru-I-Ru bond angle (126.00(2)°) in 8 is practically the same as that (125.97(2)°) found in the analogous structure of 4 in Scheme 2.
    • Despite the presence of an intervening octahedral calcium fragment, the Ru-I-Ru bond angle (126.00(2)°) in 8 is practically the same as that (125.97(2)°) found in the analogous structure of 4 in Scheme 2.
  • 28
    • 68149116206 scopus 로고    scopus 로고
    • 2.
    • 2.
  • 29
    • 68149108554 scopus 로고    scopus 로고
    • 3 pad, 8 was obtained quantitatively.
    • 3 pad, 8 was obtained quantitatively.
  • 30
    • 68149097004 scopus 로고    scopus 로고
    • See Supporting Information
    • See Supporting Information.
  • 31
    • 68149153155 scopus 로고    scopus 로고
    • The distances between two oxygen atoms of the Cp rings in 6b and 8 are 5.44 and 4.92 Å, respectively.
    • The distances between two oxygen atoms of the Cp rings in 6b and 8 are 5.44 and 4.92 Å, respectively.
  • 32
    • 68149083105 scopus 로고    scopus 로고
    • When 2 mol % of Shvo's complex was used in the oxidation, acetophenone was formed only in 20% yield after 3 h. However, when 1 mol % of 8 was used in the oxidation, 89% of acetophenone was formed after 3 h.
    • When 2 mol % of Shvo's complex was used in the oxidation, acetophenone was formed only in 20% yield after 3 h. However, when 1 mol % of 8 was used in the oxidation, 89% of acetophenone was formed after 3 h.
  • 33
    • 68149094432 scopus 로고    scopus 로고
    • Aldehyde can react with alcohol to give the corresponding hemiacetal, which is subsequently oxidized into the ester
    • Aldehyde can react with alcohol to give the corresponding hemiacetal, which is subsequently oxidized into the ester.
  • 34
    • 68149120502 scopus 로고    scopus 로고
    • When we used 2c (4 mol %) instead of 6a in the oxidation of 1phenylethanol under the conditions of Table 1, acetophenone was obtained in quantitative yield in 3 h.
    • When we used 2c (4 mol %) instead of 6a in the oxidation of 1phenylethanol under the conditions of Table 1, acetophenone was obtained in quantitative yield in 3 h.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.