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Volumn 132, Issue 34, 2010, Pages 12133-12144

Torsionally responsive C 3-symmetric Azo dyes: Azo-hydrazone tautomerism, conformational switching, and application for chemical sensing

Author keywords

[No Author keywords available]

Indexed keywords

AMBIENT CONDITIONS; AMINE SUBSTRATES; ARYL GROUP; AZO COUPLING REACTIONS; AZO-HYDRAZONE TAUTOMERISM; BLUE SHIFT; CHEMICAL SENSING; COLOR CHANGES; COMPUTATIONAL STUDIES; CONFORMATIONAL SWITCHING; DONOR ABILITY; ELECTRONIC TRANSITION; HEXYLAMINE; HOMOLOGOUS SERIES; HYDRAZONES; HYDROGEN BONDINGS; INTRAMOLECULAR HYDROGEN; LOW ENERGIES; MOLECULAR CORE; NAKED-EYE DETECTION; NMR SPECTROSCOPY; PHLOROGLUCINOL; SPECTRAL SHIFT; STRUCTURAL DISTORTIONS; SYMMETRIC MOLECULES; TORSIONAL ANGLE; TRIETHYLAMINES; TWISTING MOTION; VOLATILE AMINES;

EID: 77956087801     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja105121z     Document Type: Article
Times cited : (110)

References (123)
  • 5
    • 34248326379 scopus 로고    scopus 로고
    • Thematic issue on organic electronics and optoelectronics:, - 1386
    • Thematic issue on organic electronics and optoelectronics: Chem. Rev. 2007, 107, 923 - 1386.
    • (2007) Chem. Rev. , vol.107 , pp. 923
  • 12
    • 33746217461 scopus 로고    scopus 로고
    • For recent reviews on boron-containing π-conjugation and its modification by interaction with Lewis bases, see
    • For recent reviews on boron-containing π-conjugation and its modification by interaction with Lewis bases, see: Yamaguchi, S. and Wakamiya, A. Pure Appl. Chem. 2006, 78, 1413-1424
    • (2006) Pure Appl. Chem. , vol.78 , pp. 1413-1424
    • Yamaguchi, S.1    Wakamiya, A.2
  • 16
    • 33645699748 scopus 로고    scopus 로고
    • For selected examples of covalent modification of rigid π-skeletons with main-group elements, see
    • For selected examples of covalent modification of rigid π-skeletons with main-group elements, see: Yamaguchi, S., Xu, C., and Okamoto, T. Pure Appl. Chem. 2006, 78, 721-730
    • (2006) Pure Appl. Chem. , vol.78 , pp. 721-730
    • Yamaguchi, S.1    Xu, C.2    Okamoto, T.3
  • 26
    • 1242274597 scopus 로고    scopus 로고
    • For binding-induced conformational switching of linearly π-conjugated molecules, see
    • For binding-induced conformational switching of linearly π-conjugated molecules, see: Inouye, M., Waki, M., and Abe, H. J. Am. Chem. Soc. 2004, 126, 2022-2027
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 2022-2027
    • Inouye, M.1    Waki, M.2    Abe, H.3
  • 55
    • 0001288990 scopus 로고
    • A particular subclass of this structural motif having sugar-appended phenyl groups, known as Yariv reagents, have found practical applications in biochemical assays as multivalent dyes for staining or isolating proteoglycans. See
    • A particular subclass of this structural motif having sugar-appended phenyl groups, known as Yariv reagents, have found practical applications in biochemical assays as multivalent dyes for staining or isolating proteoglycans. See: Yariv, J., Rapport, M. M., and Graf, L. Biochem. J. 1962, 85, 383-388
    • (1962) Biochem. J. , vol.85 , pp. 383-388
    • Yariv, J.1    Rapport, M.M.2    Graf, L.3
  • 59
    • 0004267777 scopus 로고    scopus 로고
    • Royal Society of Chemistry: Cambridge, U.K
    • Christie, R. M. Colour Chemistry; Royal Society of Chemistry: Cambridge, U.K., 2001.
    • (2001) Colour Chemistry
    • Christie, R.M.1
  • 73
    • 77956090141 scopus 로고    scopus 로고
    • In a manner similar to the σ-bond cooperativity that is typically observed in extended networks of alcohols and phenols, this arrangement should polarize the participating O-H bonds and further strengthen the hydrogen bond
    • In a manner similar to the σ-bond cooperativity that is typically observed in extended networks of alcohols and phenols, this arrangement should polarize the participating O-H bonds and further strengthen the hydrogen bond.
  • 74
  • 75
    • 77956084002 scopus 로고    scopus 로고
    • CSD, version 5.31 (last updates Feb 2010)
    • CSD, version 5.31 (last updates Feb 2010).
  • 82
    • 77956084583 scopus 로고    scopus 로고
    • CSD codes: BEKHAB, BIHNUC, CABWAE, CICCUN, DEHMIN, DEHMOT, DEHMUZ, DEHNAG, DEHNEK, DEHNIO, DEHNOU, DEHNUA, DEHPAI, DOTQIN, DUNION, HIQZOX, JARPEX, JATJIX, JAYREH, KAQSAW, KIBJOU, LEMQID, LEZHIH, LEZHON, MAMMEU, MAMMIY, NQNCPH, OGUWES, OGUXAP, OLOCAT, PAHGUB, PAMBOO, POYSUS, POYTAZ, POYTED, SCNPHO, SIWVUP, SOQQIY, VEHXIP, VEHXOV, WIKWOC, WIKWUI, WIKXAP, WIKXET, ZUCQET, ZUCQIX, ZUCQOD, ZUCQUJ, ZUCRAQ
    • CSD codes: BEKHAB, BIHNUC, CABWAE, CICCUN, DEHMIN, DEHMOT, DEHMUZ, DEHNAG, DEHNEK, DEHNIO, DEHNOU, DEHNUA, DEHPAI, DOTQIN, DUNION, HIQZOX, JARPEX, JATJIX, JAYREH, KAQSAW, KIBJOU, LEMQID, LEZHIH, LEZHON, MAMMEU, MAMMIY, NQNCPH, OGUWES, OGUXAP, OLOCAT, PAHGUB, PAMBOO, POYSUS, POYTAZ, POYTED, SCNPHO, SIWVUP, SOQQIY, VEHXIP, VEHXOV, WIKWOC, WIKWUI, WIKXAP, WIKXET, ZUCQET, ZUCQIX, ZUCQOD, ZUCQUJ, ZUCRAQ.
  • 94
    • 77956070008 scopus 로고    scopus 로고
    • obs
    • obs.
  • 102
    • 0003998388 scopus 로고    scopus 로고
    • 90 th ed. (Internet version 2010); Lide D.R. Ed.; CRC Press/Taylor and Francis: Boca Raton, FL
    • CRC Handbook of Chemistry and Physics, 90 th ed. (Internet version 2010); Lide, D. R., Ed.; CRC Press/Taylor and Francis: Boca Raton, FL, 2010.
    • (2010) CRC Handbook of Chemistry and Physics
  • 113
    • 77956065391 scopus 로고    scopus 로고
    • Bruker Analytical X-Ray Systems: Madison, WI
    • SAINT; Bruker Analytical X-Ray Systems: Madison, WI, 2009.
    • (2009) SAINT
  • 116
    • 77956093851 scopus 로고    scopus 로고
    • version 7.0; Schrodinger, LLC: New York
    • Jaguar, version 7.0; Schrodinger, LLC: New York, 2007.
    • (2007) Jaguar


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.