메뉴 건너뛰기




Volumn 74, Issue 5, 2009, Pages 2080-2087

A versatile synthesis of electroactive stilbenoprismands for effective binding of metal cations

Author keywords

[No Author keywords available]

Indexed keywords

C-C BONDS; CATION RADICALS; COUPLING REACTIONS; ELECTROACTIVE; ELECTRON-RICH; ELECTRONIC COUPLINGS; H NMR SPECTROSCOPIES; METAL CATIONS; NEW CLASS; OPTICAL METHODS; POLYAROMATIC; SILVER CATIONS; X-RAY STRUCTURES;

EID: 64249173353     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo802579f     Document Type: Article
Times cited : (24)

References (43)
  • 18
    • 38949106877 scopus 로고    scopus 로고
    • Compare: Emond, S. J.; Debroy, P.; Rathore, R. Org. Lett. 2008, 10, 389.
    • Compare: Emond, S. J.; Debroy, P.; Rathore, R. Org. Lett. 2008, 10, 389.
  • 26
    • 64249132063 scopus 로고    scopus 로고
    • With the exception of the slight broadening in the first spectrum in Figure 1 with 0.2 equiv of Ag, which may arise due to the low concentration of [SB2, Ag+, the other spectra in Figure 1 did not show any significant line broadening to allow the extraction of a reliable Kd value. Compare: Rathore, R, Chebny, V. J, Abdelwahed, S. H. J. Am. Chem. Soc. 2004, 127, 8012
    • d value. Compare: Rathore, R.; Chebny, V. J.; Abdelwahed, S. H. J. Am. Chem. Soc. 2004, 127, 8012.
  • 28
    • 84869263228 scopus 로고    scopus 로고
    • 3Ag in anhydrous dichloromethane (in the absence of methanol) produced a colored solution of the SB4 cation radical as judged by spectrophotometric analysis.
    • 3Ag in anhydrous dichloromethane (in the absence of methanol) produced a colored solution of the SB4 cation radical as judged by spectrophotometric analysis.
  • 29
    • 64249086950 scopus 로고    scopus 로고
    • Owing to the poor solubility of SB1, it was not utilized in the subsequent studies.
    • (b) Owing to the poor solubility of SB1, it was not utilized in the subsequent studies.
  • 33
    • 85178352889 scopus 로고    scopus 로고
    • + using a larger counter anion, e.g., see: Nelsen, S. F.; Ismagilov, R. F.; Powell, D. R. J. Am. Chem. Soc. 1997, 119, 10213.
    • + using a larger counter anion, e.g., see: Nelsen, S. F.; Ismagilov, R. F.; Powell, D. R. J. Am. Chem. Soc. 1997, 119, 10213.
  • 34
    • 84869279414 scopus 로고    scopus 로고
    • The ideal values for the sum of the intracyclic bond angles for the planar rings are the following: 3 × 60 = 180° for 3-membered cycles, 4 × 90 = 360° for 4-membered cycles, 5 × 108 = 540° for 5-membered cycles, 6 × 120 = 720° for 6-rnemhered cycles, etc. A deviation from the ideal value of the sum of the intracyclic bond angles results either in the nonplanar conformations (e.g., the chair conformation of cyclohexane) or distortion of the bonds (e.g., the banana bonds in cyclopropane).
    • The ideal values for the sum of the intracyclic bond angles for the planar rings are the following: 3 × 60 = 180° for 3-membered cycles, 4 × 90 = 360° for 4-membered cycles, 5 × 108 = 540° for 5-membered cycles, 6 × 120 = 720° for 6-rnemhered cycles, etc. A deviation from the ideal value of the sum of the intracyclic bond angles results either in the nonplanar conformations (e.g., the chair conformation of cyclohexane) or distortion of the bonds (e.g., the "banana" bonds in cyclopropane).
  • 38
    • 35348838961 scopus 로고    scopus 로고
    • Comparera Banerjee, M.; Emond, S. J.; Lindeman, S. V.; Rathore, R J. Org. Chem. 2007, 72, 8054.
    • Comparera) Banerjee, M.; Emond, S. J.; Lindeman, S. V.; Rathore, R J. Org. Chem. 2007, 72, 8054.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.