메뉴 건너뛰기




Volumn 48, Issue 1, 1999, Pages 69-78

Classification of organic molecules to obtain electron affinities from half-wave reduction potentials: Cytosine, uracil, thymine, guanine and adenine

Author keywords

CURES EC; DNA; Electron affinity; Half wave reduction potentials; Multiconfiguration configuration interaction (MCCI)

Indexed keywords

DNA; HYDROGEN BONDS; MOLECULAR STRUCTURE; VITAMINS;

EID: 0033035657     PISSN: 03024598     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0302-4598(98)00211-6     Document Type: Article
Times cited : (39)

References (23)
  • 1
  • 2
    • 0025788223 scopus 로고
    • The determination of absolute electron affinities of the purines and pyrimidines in DNA and RNA from reversible reduction potentials
    • Wiley J.R., Robinson J.M., Ehdaie S., Chen E.C.M., Chen E.S.D., Wentworth W.E. The determination of absolute electron affinities of the purines and pyrimidines in DNA and RNA from reversible reduction potentials. Biochem. Biophys. Res. Commun. 180:1991;841-845.
    • (1991) Biochem. Biophys. Res. Commun. , vol.180 , pp. 841-845
    • Wiley, J.R.1    Robinson, J.M.2    Ehdaie, S.3    Chen, E.C.M.4    Chen, E.S.D.5    Wentworth, W.E.6
  • 3
    • 0029610425 scopus 로고
    • The experimental hardness and electronegativity of the purines and pyrimidines in DNA and RNA supported by the AM1 calculation of the electron affinities and ionization potentials
    • Zhang O., Chen E.C.M. The experimental hardness and electronegativity of the purines and pyrimidines in DNA and RNA supported by the AM1 calculation of the electron affinities and ionization potentials. Biochem. Biophys. Res. Commun. 217:1995;755-760.
    • (1995) Biochem. Biophys. Res. Commun. , vol.217 , pp. 755-760
    • Zhang, O.1    Chen, E.C.M.2
  • 5
    • 36749114988 scopus 로고
    • Negative ions and electron affinities
    • Nenner I., Schulz G.J. Negative ions and electron affinities. J. Chem. Phys. 62:1975;1747-1758.
    • (1975) J. Chem. Phys. , vol.62 , pp. 1747-1758
    • Nenner, I.1    Schulz, G.J.2
  • 6
    • 0010393644 scopus 로고
    • Formation of negative ions under inverted field ionization conditions
    • Anbar M., St. John G.A. Formation of negative ions under inverted field ionization conditions. Science. 190:1975;781-782.
    • (1975) Science , vol.190 , pp. 781-782
    • Anbar, M.1    St. John, G.A.2
  • 7
    • 0000617357 scopus 로고    scopus 로고
    • Dipole bound, nucleic acid base anions studied via negative ion photoelectron spectroscopy
    • Hendricks J.H., Lyapustina S.A., deClerq H.L., Snodgrass J.T., Bowen K.H. Dipole bound, nucleic acid base anions studied via negative ion photoelectron spectroscopy. J. Chem. Phys. 104:1996;7788-7791.
    • (1996) J. Chem. Phys. , vol.104 , pp. 7788-7791
    • Hendricks, J.H.1    Lyapustina, S.A.2    Declerq, H.L.3    Snodgrass, J.T.4    Bowen, K.H.5
  • 10
    • 33751155346 scopus 로고
    • Ab initio molecular orbital calculation of DNA radical ions: 5. Scaling of calculated electron affinities and ionization potentials to experimental values
    • Sevila M.D., Besler B., Colson A.O. Ab initio molecular orbital calculation of DNA radical ions: 5. Scaling of calculated electron affinities and ionization potentials to experimental values. J. Phys. Chem. 99:1995;1060-1063.
    • (1995) J. Phys. Chem. , vol.99 , pp. 1060-1063
    • Sevila, M.D.1    Besler, B.2    Colson, A.O.3
  • 11
    • 0032144904 scopus 로고    scopus 로고
    • A proposed model for electron conduction in DNA based upon pairwise and anion Pi stacking: Electron affinities and ionization potentials of the hydrogen bonded base pairs
    • Chen E.S.D., Chen E.C.M. A proposed model for electron conduction in DNA based upon pairwise and anion Pi stacking: electron affinities and ionization potentials of the hydrogen bonded base pairs. Bioelectrochem. Bioenergetics. 46:1998;15-18.
    • (1998) Bioelectrochem. Bioenergetics. , vol.46 , pp. 15-18
    • Chen, E.S.D.1    Chen, E.C.M.2
  • 12
    • 0029309264 scopus 로고
    • Relationship between the electron affinities and half-wave reduction potentials of fullerenes, aromatic hydrocarbons, and metal complexes
    • Ruoff R.S., Kadish K.M., Boulas P., Chen E.C.M. Relationship between the electron affinities and half-wave reduction potentials of fullerenes, aromatic hydrocarbons, and metal complexes. J. Phys. Chem. 99:1995;8843-8850.
    • (1995) J. Phys. Chem. , vol.99 , pp. 8843-8850
    • Ruoff, R.S.1    Kadish, K.M.2    Boulas, P.3    Chen, E.C.M.4
  • 13
    • 0001298277 scopus 로고
    • Solvation of anion radicals
    • Shalev H., Evans D.H. Solvation of anion radicals. J. Am. Chem. Soc. 111:1989;2667-2673.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 2667-2673
    • Shalev, H.1    Evans, D.H.2
  • 14
    • 33947294820 scopus 로고
    • Ground states of conjugated molecules: XXII. Polarographic reduction potentials of hydrocarbons
    • Dewar M.J.S., Hashmall J.A., Trinjstic N. Ground states of conjugated molecules: XXII. Polarographic reduction potentials of hydrocarbons. J. Am. Chem. Soc. 92:1970;5555-5559.
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 5555-5559
    • Dewar, M.J.S.1    Hashmall, J.A.2    Trinjstic, N.3
  • 15
    • 0032496044 scopus 로고    scopus 로고
    • The electron affinities of the radicals formed by the loss of an aromatic hydrogen atom from AGCUT
    • Chen E.S.D., Chen E.C.M., Sane N. The electron affinities of the radicals formed by the loss of an aromatic hydrogen atom from AGCUT. Biochem. Biophys. Res. Commun. 246:1998;228-230.
    • (1998) Biochem. Biophys. Res. Commun. , vol.246 , pp. 228-230
    • Chen, E.S.D.1    Chen, E.C.M.2    Sane, N.3
  • 17
    • 0242454162 scopus 로고
    • Electron affinities and electron transfer reactions
    • Kebarle P., Chowdhury S. Electron affinities and electron transfer reactions. Chem. Rev. 87:1987;513-554.
    • (1987) Chem. Rev. , vol.87 , pp. 513-554
    • Kebarle, P.1    Chowdhury, S.2
  • 19
    • 0000445880 scopus 로고    scopus 로고
    • Comment on Ionization Potentials and Electron Affinities from the Extended Koopmans' Theorem Applied to Energy Derivative Density Matrices: The EKTMPn and EKTQCISD methods
    • [J. Cioslowski, P. Piskorz, G. Liu
    • E.S.D. Chen, E.C.M. Chen, Comment on Ionization Potentials and Electron Affinities from the Extended Koopmans' Theorem Applied to Energy Derivative Density Matrices: The EKTMPn and EKTQCISD methods [J. Cioslowski, P. Piskorz, G. Liu J. Chem. Phys. 107, 6804 (1997)], 108 (1998), pp. 8749-8750.
    • (1997) J. Chem. Phys. , vol.107 , pp. 6804
    • Chen, E.S.D.1    Chen, E.C.M.2
  • 20
    • 0344387522 scopus 로고    scopus 로고
    • E.S.D. Chen, E.C.M. Chen, Comment on Ionization Potentials and Electron Affinities from the Extended Koopmans' Theorem Applied to Energy Derivative Density Matrices: The EKTMPn and EKTQCISD methods [J. Cioslowski, P. Piskorz, G. Liu J. Chem. Phys. 107, 6804 (1997)], 108 (1998), pp. 8749-8750.
    • (1998) J. Chem. Phys. , vol.108 , pp. 8749-8750
  • 21
    • 0000566836 scopus 로고
    • Formation of the radical anion of cubene and the determination of the heat of formation, heat of hydrogenation, and olefin strain energy of cubene
    • Staneke P.O., Ingemann S., Emrick T., Eaton P., Nibbering N.M.M., Kass S.R. Formation of the radical anion of cubene and the determination of the heat of formation, heat of hydrogenation, and olefin strain energy of cubene. J. Am. Chem. Soc. 116:1994;6445-6446.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 6445-6446
    • Staneke, P.O.1    Ingemann, S.2    Emrick, T.3    Eaton, P.4    Nibbering, N.M.M.5    Kass, S.R.6
  • 22
    • 0031048782 scopus 로고    scopus 로고
    • Cubyl anion formation and an experimental determination of the acidity and C-H bond dissociation energy of cubane
    • Hare M., Emrick T., Eaton P., Kass S.R. Cubyl anion formation and an experimental determination of the acidity and C-H bond dissociation energy of cubane. J. Am. Chem. Soc. 119:1997;121-122.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 121-122
    • Hare, M.1    Emrick, T.2    Eaton, P.3    Kass, S.R.4
  • 23
    • 0000364937 scopus 로고    scopus 로고
    • Photoinduced electron transfer to pyrimidines and 5,6 dihydropyrimidine derivatives reduction potentials determined by florescence quenching kinetics
    • Scannell M.P., Prakash G., Fahley D.E. Photoinduced electron transfer to pyrimidines and 5,6 dihydropyrimidine derivatives reduction potentials determined by florescence quenching kinetics. J. Phys. Chem. A. 101:1997;4332-4340.
    • (1997) J. Phys. Chem. A. , vol.101 , pp. 4332-4340
    • Scannell, M.P.1    Prakash, G.2    Fahley, D.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.