메뉴 건너뛰기




Volumn 17, Issue 13, 1998, Pages 2689-2691

Synthesis and reactions of fac-Re(bpy)(CO)3(CH2OR) (R = H, acetyl; bpy = 2,2′-bipyridyl)

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001109512     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om980102m     Document Type: Article
Times cited : (30)

References (47)
  • 15
    • 0000221722 scopus 로고
    • See, for example: (a) Ishida, H.; Tanaka, K.; Morimoto, M.; Tanaka, T. Organometallics 1986, 5, 724. (b) Tanaka, H.; Nagao, H.; Peng, S.-M.; Tanaka, K. Organometallics 1992, 11, 1450. (c) Tanaka, H.; Tzeng, B.-C.; Nagao, H.; Peng, S.-M.; Tanaka, K. Inorg. Chem. 1993, 32, 1508. (d) Toyohara, K.; Nagao, H.; Adachi, T.; Yoshida, T.; Tanaka, K. Chem. Lett. 1996, 27. (e) Hankka, M.; Kiviaho, J.; Ahlgren, M.; Pakkanen, T. A. Organometallics 1995, 14, 825.
    • (1986) Organometallics , vol.5 , pp. 724
    • Ishida, H.1    Tanaka, K.2    Morimoto, M.3    Tanaka, T.4
  • 16
    • 0001029702 scopus 로고
    • See, for example: (a) Ishida, H.; Tanaka, K.; Morimoto, M.; Tanaka, T. Organometallics 1986, 5, 724. (b) Tanaka, H.; Nagao, H.; Peng, S.-M.; Tanaka, K. Organometallics 1992, 11, 1450. (c) Tanaka, H.; Tzeng, B.-C.; Nagao, H.; Peng, S.-M.; Tanaka, K. Inorg. Chem. 1993, 32, 1508. (d) Toyohara, K.; Nagao, H.; Adachi, T.; Yoshida, T.; Tanaka, K. Chem. Lett. 1996, 27. (e) Hankka, M.; Kiviaho, J.; Ahlgren, M.; Pakkanen, T. A. Organometallics 1995, 14, 825.
    • (1992) Organometallics , vol.11 , pp. 1450
    • Tanaka, H.1    Nagao, H.2    Peng, S.-M.3    Tanaka, K.4
  • 17
    • 33751386331 scopus 로고
    • See, for example: (a) Ishida, H.; Tanaka, K.; Morimoto, M.; Tanaka, T. Organometallics 1986, 5, 724. (b) Tanaka, H.; Nagao, H.; Peng, S.-M.; Tanaka, K. Organometallics 1992, 11, 1450. (c) Tanaka, H.; Tzeng, B.-C.; Nagao, H.; Peng, S.-M.; Tanaka, K. Inorg. Chem. 1993, 32, 1508. (d) Toyohara, K.; Nagao, H.; Adachi, T.; Yoshida, T.; Tanaka, K. Chem. Lett. 1996, 27. (e) Hankka, M.; Kiviaho, J.; Ahlgren, M.; Pakkanen, T. A. Organometallics 1995, 14, 825.
    • (1993) Inorg. Chem. , vol.32 , pp. 1508
    • Tanaka, H.1    Tzeng, B.-C.2    Nagao, H.3    Peng, S.-M.4    Tanaka, K.5
  • 18
    • 20544447483 scopus 로고    scopus 로고
    • See, for example: (a) Ishida, H.; Tanaka, K.; Morimoto, M.; Tanaka, T. Organometallics 1986, 5, 724. (b) Tanaka, H.; Nagao, H.; Peng, S.-M.; Tanaka, K. Organometallics 1992, 11, 1450. (c) Tanaka, H.; Tzeng, B.-C.; Nagao, H.; Peng, S.-M.; Tanaka, K. Inorg. Chem. 1993, 32, 1508. (d) Toyohara, K.; Nagao, H.; Adachi, T.; Yoshida, T.; Tanaka, K. Chem. Lett. 1996, 27. (e) Hankka, M.; Kiviaho, J.; Ahlgren, M.; Pakkanen, T. A. Organometallics 1995, 14, 825.
    • (1996) Chem. Lett. , pp. 27
    • Toyohara, K.1    Nagao, H.2    Adachi, T.3    Yoshida, T.4    Tanaka, K.5
  • 19
    • 0029252180 scopus 로고
    • See, for example: (a) Ishida, H.; Tanaka, K.; Morimoto, M.; Tanaka, T. Organometallics 1986, 5, 724. (b) Tanaka, H.; Nagao, H.; Peng, S.-M.; Tanaka, K. Organometallics 1992, 11, 1450. (c) Tanaka, H.; Tzeng, B.-C.; Nagao, H.; Peng, S.-M.; Tanaka, K. Inorg. Chem. 1993, 32, 1508. (d) Toyohara, K.; Nagao, H.; Adachi, T.; Yoshida, T.; Tanaka, K. Chem. Lett. 1996, 27. (e) Hankka, M.; Kiviaho, J.; Ahlgren, M.; Pakkanen, T. A. Organometallics 1995, 14, 825.
    • (1995) Organometallics , vol.14 , pp. 825
    • Hankka, M.1    Kiviaho, J.2    Ahlgren, M.3    Pakkanen, T.A.4
  • 23
    • 11644309057 scopus 로고    scopus 로고
    • note
    • 3OD): δ 203.98, 194.44, 156.59, 153.74, 139.24, 127.80, 124.68, 70.05.
  • 24
    • 11644254740 scopus 로고    scopus 로고
    • note
    • 3CN): δ 203.06, 194.37, 171.70, 156.29, 153.89, 139.52, 127.96, 124.40, 69.33, 20.98.
  • 25
    • 85087242539 scopus 로고    scopus 로고
    • note
    • 1/n; a = 9.7402(2) A, b = 15.8826(4) A°, c = 11.2409(2) A°, α= 90°, β= 107.905(1)°, γ= 90°. Final R indices (I > 2σ(I)): R1 = 0.0390, wR2 = 0.0768.
  • 26
    • 11644291314 scopus 로고    scopus 로고
    • note
    • Additional commentary about the structure and ORTEP packing diagrams are available in the Supporting Information.
  • 27
    • 11644258587 scopus 로고    scopus 로고
    • note
    • 3OD): δ 199.97, 194.26, 157.50, 154.07, 141.24, 128.60, 125.07, 61.60.
  • 28
    • 11644274804 scopus 로고    scopus 로고
    • note
    • 12
  • 29
    • 0004150157 scopus 로고
    • Program Library for Structure Solution and Molecular Graphics; Siemens Analytical Instruments Division: Madison, WI
    • SHELXTL 5.03 (PC-version), Program Library for Structure Solution and Molecular Graphics; Siemens Analytical Instruments Division: Madison, WI, 1995.
    • (1995) SHELXTL 5.03 (PC-version)
  • 30
    • 33947338539 scopus 로고    scopus 로고
    • note
    • 4, the formaldehyde hemiacetal is present in low yield (diminished by partial removal with solvent).
  • 31
    • 0004284856 scopus 로고
    • McGraw Hill: Maidenhead, England
    • Addition of dimedone to the mixture results in slow disappearance of the resonance at δ 4.64 and formation of the dimedoneformaldehyde derivative (compared with an authentic sample: Kemp, W. Qualitative Organic Analysis; McGraw Hill: Maidenhead, England, 1986; p 89).
    • (1986) Qualitative Organic Analysis , pp. 89
    • Kemp, W.1
  • 40
    • 11644284980 scopus 로고    scopus 로고
    • note
    • 4; after filtration, the filtrate was concentrated to 20 mL. Hexane was then added to effect precipitation of 0.34 g (83% yield) of 5.
  • 42
    • 11644264038 scopus 로고    scopus 로고
    • note
    • 1H NMR showed an acetoxy methyl resonance at δ 1.91 and resonances for bipyridyl protons which are distinct from 6; the ratio of the two compounds was 2:1 of the unknown to 6). Continued photolysis, or evaporation of solvent and redissolution, resulted in conversion of the second compound to 6. Samples were too dilute to provide meaningful IR spectral data.
  • 43
    • 11644264471 scopus 로고    scopus 로고
    • note
    • 2 had identical spectral properties.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.