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Volumn 8, Issue 3, 2009, Pages 309-311

Excited-state acidity of the 8-hydroxyacridizinium ion - A water-soluble photoacid

Author keywords

[No Author keywords available]

Indexed keywords

8 HYDROXYACRIDIZINIUM; ACID; UNCLASSIFIED DRUG;

EID: 61649091120     PISSN: 1474905X     EISSN: 14749092     Source Type: Journal    
DOI: 10.1039/b816048a     Document Type: Article
Times cited : (9)

References (24)
  • 1
    • 0001139129 scopus 로고
    • Fast reactions of excited molecules
    • A. Weller Fast reactions of excited molecules Prog. React. Kinet. 1961 1 187
    • (1961) Prog. React. Kinet. , vol.1 , pp. 187
    • Weller, A.1
  • 2
    • 0005388526 scopus 로고
    • Acid-Base Properties of Electronically Excited States of Organic Molecules
    • J. F. Ireland P. A. H. Wyatt Acid-Base Properties of Electronically Excited States of Organic Molecules Adv. Phys. Org. Chem 1976 12 131
    • (1976) Adv. Phys. Org. Chem , vol.12 , pp. 131
    • Ireland, J.F.1    Wyatt, P.A.H.2
  • 3
    • 0001769521 scopus 로고
    • Excited-State Proton-Transfer Reactions: 1. Fundamentals and Intermolecular Reactions
    • L. G. Arnaut S. J. Formosinho Excited-State Proton-Transfer Reactions: 1. Fundamentals and Intermolecular Reactions J. Photochem. Photobiol. A 1993 75 1
    • (1993) J. Photochem. Photobiol. A , vol.75 , pp. 1
    • Arnaut, L.G.1    Formosinho, S.J.2
  • 4
    • 0036149612 scopus 로고    scopus 로고
    • Excited-State Proton Transfer: From Constrained Systems to "super" Photoacids to Superfast Proton Transfer
    • L. M. Tolbert K. M. Solntsev Excited-State Proton Transfer: From Constrained Systems to "Super" Photoacids to Superfast Proton Transfer Acc. Chem. Res. 2002 35 19
    • (2002) Acc. Chem. Res. , vol.35 , pp. 19
    • Tolbert, L.M.1    Solntsev, K.M.2
  • 5
    • 12344331638 scopus 로고    scopus 로고
    • Elementary Steps in Excited-State Proton Transfer
    • See e.g.
    • N. Agmon Elementary Steps in Excited-State Proton Transfer J. Phys. Chem. A 2005 109 13
    • (2005) J. Phys. Chem. A , vol.109 , pp. 13
    • Agmon, N.1
  • 6
    • 45549093762 scopus 로고    scopus 로고
    • Photosensitized Tetrahydropyran Transfer
    • R. P. Oates Paul B. Jones Photosensitized Tetrahydropyran Transfer J. Org. Chem. 2008 73 4743
    • (2008) J. Org. Chem. , vol.73 , pp. 4743
    • Oates, R.P.1    Jones Paul, B.2
  • 7
    • 0037471648 scopus 로고    scopus 로고
    • Novel Photoacid Generators for Photodirected Oligonucleotide Synthesis
    • See e.g.
    • P. J. Serafinowski P. B. Garland Novel Photoacid Generators for Photodirected Oligonucleotide Synthesis J. Am. Chem. Soc. 2003 125 962
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 962
    • Serafinowski, P.J.1    Garland, P.B.2
  • 8
    • 0342862136 scopus 로고
    • Photoinduced Coupled Proton and Electron Transfers. 1. 6-Hydroxyquinoline
    • E. Bardez A. Chatelain B. Larrey B. Valeur Photoinduced Coupled Proton and Electron Transfers. 1. 6-Hydroxyquinoline J. Phys. Chem. 1994 98 2357
    • (1994) J. Phys. Chem. , vol.98 , pp. 2357
    • Bardez, E.1    Chatelain, A.2    Larrey, B.3    Valeur, B.4
  • 9
    • 0035799968 scopus 로고    scopus 로고
    • Catalytic Roles of Water Protropic Species in the Tautomerization of Excited 6-Hydroxyquinoline: Migration of Hydrated Proton Clusters
    • T. G. Kim Y. Kim D.-J. Jang Catalytic Roles of Water Protropic Species in the Tautomerization of Excited 6-Hydroxyquinoline: Migration of Hydrated Proton Clusters J. Phys. Chem. A 2001 105 4328
    • (2001) J. Phys. Chem. A , vol.105 , pp. 4328
    • Kim, T.G.1    Kim, Y.2    Jang, D.-J.3
  • 10
    • 1642341914 scopus 로고    scopus 로고
    • Picosecond Dynamics of the Photoexcited 6-Methoxyquinoline and 6-Hydroxyquinoline Molecules in Solution
    • O. Poizat E. Bardez G. Buntinx V. Alain Picosecond Dynamics of the Photoexcited 6-Methoxyquinoline and 6-Hydroxyquinoline Molecules in Solution J. Phys. Chem. A 2004 108 1873
    • (2004) J. Phys. Chem. A , vol.108 , pp. 1873
    • Poizat, O.1    Bardez, E.2    Buntinx, G.3    Alain, V.4
  • 12
    • 6744272590 scopus 로고
    • Aromatic Cyclodehydration. XXXV.1 Alkoxyl Derivatives of the Acridizinium Ion
    • For a biaryl-type photoacid with a pyridinium substituent see:
    • C. K. Bradsher J. H. Jones Aromatic Cyclodehydration. XXXV.1 Alkoxyl Derivatives of the Acridizinium Ion J. Am. Chem. Soc. 1957 79 6033
    • (1957) J. Am. Chem. Soc. , vol.79 , pp. 6033
    • Bradsher, C.K.1    Jones, J.H.2
  • 14
    • 0034604509 scopus 로고    scopus 로고
    • New Dyes Based on Amino-Substituted Acridizinium Salts-Synthesis and Exceptional Photochemical Properties
    • H. Ihmels K. Faulhaber B. Engels C. Lennartz New Dyes Based on Amino-Substituted Acridizinium Salts-Synthesis and Exceptional Photochemical Properties Chem.-Eur. J. 2000 6 2854
    • (2000) Chem.-Eur. J. , vol.6 , pp. 2854
    • Ihmels, H.1    Faulhaber, K.2    Engels, B.3    Lennartz, C.4
  • 15
    • 41749109318 scopus 로고    scopus 로고
    • Water-soluble, pH-sensitive fluorescent probes on the basis of acridizinium ions
    • A. Bergen A. Granzhan H. Ihmels Water-soluble, pH-sensitive fluorescent probes on the basis of acridizinium ions Photochem. Photobiol. Sci. 2008 7 405
    • (2008) Photochem. Photobiol. Sci. , vol.7 , pp. 405
    • Bergen, A.1    Granzhan, A.2    Ihmels, H.3
  • 20
    • 1842332527 scopus 로고
    • Electrophilic Substituent Constants, the Effect of Structure upon the Reactions of Organic Compounds. Benzene Derivatives
    • H. C. Brown Y. Okamoto Electrophilic Substituent Constants, The Effect of Structure upon the Reactions of Organic Compounds. Benzene Derivatives J. Am. Chem. Soc. 1958 80 4979
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 4979
    • Brown, H.C.1    Okamoto, Y.2
  • 21
    • 0002801544 scopus 로고
    • The Effect of Structure upon the Reactions of Organic Compounds. Benzene Derivatives
    • L. P. Hammett The Effect of Structure upon the Reactions of Organic Compounds. Benzene Derivatives J. Am. Chem. Soc. 1937 59 96
    • (1937) J. Am. Chem. Soc. , vol.59 , pp. 96
    • Hammett, L.P.1
  • 22
    • 33846238619 scopus 로고    scopus 로고
    • Acridizinium salts. Preparation from 1-(benzylic)-2-formyl and 1-(benzylic)-2-acetyl pyridinium bromides and ring-openings reactions with nucleophilic reagents
    • A. P. Krapcho S. A. Cadamuro L. Macnee Acridizinium salts. Preparation from 1-(benzylic)-2-formyl and 1-(benzylic)-2-acetyl pyridinium bromides and ring-openings reactions with nucleophilic reagents ARKIVOC 2007 ix 28
    • (2007) ARKIVOC , vol.9 , pp. 28
    • Krapcho, A.P.1    Cadamuro, S.A.2    MacNee, L.3
  • 23
    • 0141662585 scopus 로고
    • Acridizinium Ion Chemistry. VI. Reaction, with Bases. II
    • C. K. Bradsher J. P. Sherer Acridizinium Ion Chemistry. VI. Reaction, with Bases. II J. Org. Chem. 1967 32 733
    • (1967) J. Org. Chem. , vol.32 , pp. 733
    • Bradsher, C.K.1    Sherer, J.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.