메뉴 건너뛰기




Volumn 115, Issue 21, 2011, Pages 10797-10805

The role of intermolecular hydrogen bonding and proton transfer in proton-coupled electron transfer

Author keywords

[No Author keywords available]

Indexed keywords

1 ,4 HYDROQUINONES; DIFFUSION COEFFICIENTS; DIGITAL SIMULATION; ELECTROCHEMICAL STUDIES; H NMR SPECTROSCOPY; HALF-WAVE; HYDROGEN BONDINGS; INTERMOLECULAR HYDROGEN BONDING; KINETIC ISOTOPES; PROTON-COUPLED ELECTRON TRANSFER; REDOX POTENTIALS; THERMODYNAMIC EFFECT; TRANSITION STATE; TRIFLUOROACETATES; VOLTAMMOGRAMS;

EID: 79957793611     PISSN: 19327447     EISSN: 19327455     Source Type: Journal    
DOI: 10.1021/jp108339k     Document Type: Article
Times cited : (44)

References (69)
  • 2
    • 3042780720 scopus 로고    scopus 로고
    • Proton-Coupled Electron Transfer: A Reaction's Chemist View
    • Mayer, J. M. Proton-Coupled Electron Transfer: A Reaction's Chemist View Annu. Rev. Phys. Chem. 2007, 55, 363-390
    • (2007) Annu. Rev. Phys. Chem. , vol.55 , pp. 363-390
    • Mayer, J.M.1
  • 3
    • 49049092656 scopus 로고    scopus 로고
    • Electrochemical Approach to the Mechanistic Study of Proton-Coupled Electron Transfer
    • Costentin, C. Electrochemical Approach to the Mechanistic Study of Proton-Coupled Electron Transfer Chem. Rev. 2008, 108, 2145-2179
    • (2008) Chem. Rev. , vol.108 , pp. 2145-2179
    • Costentin, C.1
  • 4
    • 34447637309 scopus 로고    scopus 로고
    • The possible role of proton-coupled electron transfer (PCET) in water oxidation by photosystem II
    • DOI 10.1002/anie.200600917
    • Meyer, T. J.; Huynh, V. H.; Thorp, H. H. The Possible Role of Proton -Coupled Electron (PCET) in Water Oxidation by Photosystem II Angew. Chem., Int. Ed. Engl. 2007, 46, 5284-5304 (Pubitemid 47086254)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.28 , pp. 5284-5304
    • Meyer, T.J.1    Huynh, M.H.V.2    Thorp, H.H.3
  • 5
    • 77954854041 scopus 로고    scopus 로고
    • Concerted Proton-Electron Transfers: Electrochemical and Related Approaches
    • Costentin, C.; Rober, M.; Saveant, J.-M. Concerted Proton-Electron Transfers: Electrochemical and Related Approaches Acc. Chem. Res. 2010, 43, 1019-1029
    • (2010) Acc. Chem. Res. , vol.43 , pp. 1019-1029
    • Costentin, C.1    Rober, M.2    Saveant, J.-M.3
  • 6
    • 77956529755 scopus 로고    scopus 로고
    • Concerted Proton-Electron Transfers in the Oxidation of Phenols
    • Costentin, C.; Robert, M.; Saveant, J.-M. Concerted Proton-Electron Transfers in the Oxidation of Phenols Phys. Chem. Chem. Phys. 2010, 12, 11179-11190
    • (2010) Phys. Chem. Chem. Phys. , vol.12 , pp. 11179-11190
    • Costentin, C.1    Robert, M.2    Saveant, J.-M.3
  • 7
    • 33644601917 scopus 로고    scopus 로고
    • Electrochemical Concerted Proton and Electron Transfers. Potential-Dependent Rate Constant, Reorganization Factors, Proton Tunneling and Isotope Effects
    • Costentin, C.; Robert, M.; Saveant, J.-M. Electrochemical Concerted Proton and Electron Transfers. Potential-Dependent Rate Constant, Reorganization Factors, Proton Tunneling and Isotope Effects J. Electroanal. Chem. 2006, 588, 197-206
    • (2006) J. Electroanal. Chem. , vol.588 , pp. 197-206
    • Costentin, C.1    Robert, M.2    Saveant, J.-M.3
  • 8
    • 1942436066 scopus 로고    scopus 로고
    • Thermodynamics and kinetics of proton-coupled electron transfer: Stepwise vs. concerted pathways
    • DOI 10.1016/j.bbabio.2003.07.002, PII S0005272803002019
    • Mayer, J. M.; Rhile, I. J. Thermodynamics and Kinetics of Proton-Coupled Electron Transfer: Stepwise vs. Concerted Pathways Biochim. Biophys. Acta 2004, 1655, 51-58 (Pubitemid 38528743)
    • (2004) Biochimica et Biophysica Acta - Bioenergetics , vol.1655 , Issue.1-3 , pp. 51-58
    • Mayer, J.M.1    Rhile, I.J.2
  • 9
    • 38349029127 scopus 로고    scopus 로고
    • Concerted Proton-Electron Transfer in Pyridylphenols: The Importance of the Hydrogen Bond
    • Markle, T. F.; Mayer, J. M. Concerted Proton-Electron Transfer in Pyridylphenols: The Importance of the Hydrogen Bond Angew. Chem., Int. Ed. Engl. 2008, 47, 738-740
    • (2008) Angew. Chem., Int. Ed. Engl. , vol.47 , pp. 738-740
    • Markle, T.F.1    Mayer, J.M.2
  • 10
    • 42649086497 scopus 로고    scopus 로고
    • One-step versus stepwise mechanism in protonated amino acid-promoted electron-transfer reduction of a quinone by electron donors and two-electron reduction by a dihydronicotinamide adenine dinucleotide analogue. Interplay between electron transfer and hydrogen bonding
    • DOI 10.1021/ja8001452
    • Yuasa, J.; Yamada, S.; Fukuzumi, S. One-Step Versus Stepwise Mechanism in Protonated Amino Acid-Promoted Electron-Transfer Reduction of a Quinone by Electron Donors and Two-Electron Reduction by a Dihydronicotinamide Adenine Dinucleotide Analogue. Interplay Between Electron Transfer and Hydrogen Bonding J. Am. Chem. Soc. 2008, 130, 5808-5820 (Pubitemid 351600514)
    • (2008) Journal of the American Chemical Society , vol.130 , Issue.17 , pp. 5808-5820
    • Yuasa, J.1    Yamada, S.2    Fukuzumi, S.3
  • 11
    • 0001461840 scopus 로고    scopus 로고
    • Efficiency of Proton Transfer Catalysis in Models and Enzymes
    • Kirby, A. J. Efficiency of Proton Transfer Catalysis in Models and Enzymes Acc. Chem. Res. 1997, 30, 290-296 (Pubitemid 127472562)
    • (1997) Accounts of Chemical Research , vol.30 , Issue.7 , pp. 290-296
    • Kirby, A.J.1
  • 12
    • 79957828422 scopus 로고    scopus 로고
    • Acid-Base Catalysis by Enzymes
    • Cox, M. M., Ed.; John Wiley and Sons: Hoboken, NJ, 2007; Vol
    • Kirby, A. J. Acid-Base Catalysis by Enzymes. In Handbook of Proteins: Structure, Function and Methods; Cox, M. M., Ed.; John Wiley and Sons: Hoboken, NJ, 2007; Vol. 1, pp 429-435.
    • Handbook of Proteins: Structure, Function and Methods , vol.1 , pp. 429-435
    • Kirby, A.J.1
  • 13
    • 77955151113 scopus 로고    scopus 로고
    • General Acid-Base Catalysis in Model Systems
    • Hynes, J. T., Klinman, J. P., Limbach, H.-H., Schowen, R. L., Eds.; Wiley-VCH, Verlag GmbH and Co. KGaA: Weinheim, Germany,; Vol
    • Kirby, A. J. General Acid-Base Catalysis in Model Systems. In Hydrogen Transfer Reactions; Hynes, J. T., Klinman, J. P., Limbach, H.-H., Schowen, R. L., Eds.; Wiley-VCH, Verlag GmbH and Co. KGaA: Weinheim, Germany, 2007; Vol. 3, pp 975-1012.
    • (2007) Hydrogen Transfer Reactions , vol.3 , pp. 975-1012
    • Kirby, A.J.1
  • 15
    • 0037151623 scopus 로고    scopus 로고
    • Hydrogen Bonding and Catalysis of Solvolysis of 4-Methoxybenzyl Fluoride
    • Toteva, M. M.; Richard, J. P. Hydrogen Bonding and Catalysis of Solvolysis of 4-Methoxybenzyl Fluoride J. Am. Chem. Soc. 2002, 124, 9798-9805
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 9798-9805
    • Toteva, M.M.1    Richard, J.P.2
  • 16
    • 0041989850 scopus 로고    scopus 로고
    • Challenges in enzyme mechanism and energetics
    • DOI 10.1146/annurev.biochem.72.121801.161617
    • Kraut, D. A.; Carroll, K. S.; Herschlag, D. Challenges in Enzyme Mechanism and Energetics Annu. Rev. Biochem. 2003, 72, 517-571 (Pubitemid 36934521)
    • (2003) Annual Review of Biochemistry , vol.72 , pp. 517-571
    • Kraut, D.A.1    Carroll, K.S.2    Herschlag, D.3
  • 17
    • 0022418084 scopus 로고
    • Electrocatalysis of Proton-Coupled Electron-Transfer Reactions at Glassy Carbon Electrodes
    • Cabaniss, G. E.; Diamantis, A. A.; Murphy, W. R.; Linton, R. W.; Meyer, T. J. Electrocatalysis of Proton-Coupled Electron-Transfer Reactions at Glassy Carbon Electrodes J. Am. Chem. Soc. 1985, 107, 1845-1853
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 1845-1853
    • Cabaniss, G.E.1    Diamantis, A.A.2    Murphy, W.R.3    Linton, R.W.4    Meyer, T.J.5
  • 18
    • 0033568988 scopus 로고    scopus 로고
    • Control of Catechol and Hydroquinone Electron-Transfer Kinetics on Native and Modified Glassy Carbon Electrodes
    • Duvall, H. S.; McCreery, R. L. Control of Catechol and Hydroquinone Electron-Transfer Kinetics on Native and Modified Glassy Carbon Electrodes Anal. Chem. 1999, 71, 4594-4602
    • (1999) Anal. Chem. , vol.71 , pp. 4594-4602
    • Duvall, H.S.1    McCreery, R.L.2
  • 19
    • 0034686723 scopus 로고    scopus 로고
    • Self-catalysis by catechols and quinones during heterogeneous electron transfer at carbon electrodes
    • DOI 10.1021/ja000227u
    • Duvall, H. S.; McCreery, R. L. Self-Catalysis by Catechols and Quinones During Heterogenous Electron Transfer at Carbon Electrodes J. Am. Chem. Soc. 2000, 122, 6759-6764 (Pubitemid 30489998)
    • (2000) Journal of the American Chemical Society , vol.122 , Issue.28 , pp. 6759-6764
    • Duvall, S.H.1    McCreery, R.L.2
  • 20
    • 0033561723 scopus 로고    scopus 로고
    • Surface chemistry and electron-transfer kinetics of hydrogen-modified glassy carbon electrodes
    • DOI 10.1021/ac9807666
    • Kuo, T.-C.; McCreery, R. L. Surface Chemistry and Electron-transfer Kinetics of Hydrogen-Modified Glassy Electrodes Anal. Chem. 1999, 71, 1553-1560 (Pubitemid 29185964)
    • (1999) Analytical Chemistry , vol.71 , Issue.8 , pp. 1553-1560
    • Kuo, T.-C.1    McCreery, R.L.2
  • 21
    • 77957899583 scopus 로고    scopus 로고
    • Reorganization Energies and Pre-Exponential Factors in the One-Electron Electrochemical and Homogeneous Oxidation of Phenols Coupled with an Intramolecular Amine-Driven Proton Transfer
    • Costentin, C.; Robert, M.; Saveant, J.-M. Reorganization Energies and Pre-Exponential Factors in the One-Electron Electrochemical and Homogeneous Oxidation of Phenols Coupled with an Intramolecular Amine-Driven Proton Transfer Phys. Chem. Chem. Phys. 2010, 12, 13061-13069
    • (2010) Phys. Chem. Chem. Phys. , vol.12 , pp. 13061-13069
    • Costentin, C.1    Robert, M.2    Saveant, J.-M.3
  • 22
    • 77952594401 scopus 로고    scopus 로고
    • Inserting a Hydrogen-Bond Relay between Proton Exchanging Sites in Proton-Coupled Electron Transfers
    • Costentin, C.; Robert, M.; Saveant, J.-M.; Tard, C. Inserting a Hydrogen-Bond Relay Between Proton Exchanging Sites in Proton-Coupled Electron Transfers Angew. Chem., Int. Ed. 2010, 49, 3803-3806
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 3803-3806
    • Costentin, C.1    Robert, M.2    Saveant, J.-M.3    Tard, C.4
  • 23
    • 0030748041 scopus 로고    scopus 로고
    • Hydrogen-bonding and protonation effects in electrochemistry of quinones in aprotic solvents
    • DOI 10.1021/ja970028j
    • Gupta, N.; Linschitz, H. Hydrogen-Bonding and Protonation Effects in Electrochemistry of Quinones in Aprotic Solvents J. Am. Chem. Soc. 1997, 119, 6384-6391 (Pubitemid 27364252)
    • (1997) Journal of the American Chemical Society , vol.119 , Issue.27 , pp. 6384-6391
    • Gupta, N.1    Linschitz, H.2
  • 24
    • 0031585677 scopus 로고    scopus 로고
    • 60 with hydrogen-bonded phenols: Effects of solvation, deuteration, and redox potentials
    • DOI 10.1021/ja9727528
    • 60 with Hydrogen-Bonded Phenols: Effects of Solvation, Deuteration, and Redox Potentials J. Am. Chem. Soc. 1997, 119, 12601-12609 (Pubitemid 28053829)
    • (1997) Journal of the American Chemical Society , vol.119 , Issue.51 , pp. 12601-12609
    • Biczok, L.1    Gupta, N.2    Linschitz, H.3
  • 25
    • 33745961107 scopus 로고    scopus 로고
    • Carboxylates as proton-accepting groups in concerted proton-electron transfers. Electrochemistry of the 2,5-dicarboxylate 1,4-hydrobenzoquinone/2,5- dicarboxy 1,4-benzoquinone couple
    • DOI 10.1021/ja0621750
    • Costentin, C.; Robert, M.; Saveant, J.-M. Carboxylates as Proton Accepting Groups in Concerted Proton Electron Transfers. Electrochemistry of the 2,5-Dicarboxylate-1,4-Hydroxybenzoquinone/2,5-Dicarboxy-1,4-Benzoquinone Couple J. Am. Chem. Soc. 2006, 128, 8726-8727 (Pubitemid 44061520)
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.27 , pp. 8726-8727
    • Costentin, C.1    Robert, M.2    Saveant, J.-M.3
  • 26
    • 0031102572 scopus 로고    scopus 로고
    • 60 by hydrogen-bonded naphthols : Concerted electron and proton movement
    • Gupta, N.; Linschitz, H.; Biczok, L. Reduction of Triplet C60 by Hydrogen-Bonded Naphthols: Concerted Electron and Proton Movement Fullerene Sci. Technol. 1997, 5, 343-353 (Pubitemid 127554676)
    • (1997) Fullerene Science and Technology , vol.5 , Issue.2 , pp. 343-353
    • Gupta, N.1    Linschitz, H.2    Biczok, L.3
  • 27
    • 0030662641 scopus 로고    scopus 로고
    • Quenching processes in hydrogen-bonded pairs: Interactions of excited fluorenone with alcohols and phenols
    • DOI 10.1021/ja972071c
    • Biczok, L.; Berces, T.; Linschitz, H. Quenching Processes in Hydrogen-Bonded Pairs: Interactions of Excited Fluorenone with Alcohols and Phenols J. Am. Chem. Soc. 1997, 119, 11071-11077 (Pubitemid 27528853)
    • (1997) Journal of the American Chemical Society , vol.119 , Issue.45 , pp. 11071-11077
    • Biczok, L.1    Berces, T.2    Linschitz, H.3
  • 28
    • 33751154482 scopus 로고
    • Concerted Electron and Proton Movement in Quenching of Triplet C60 and Tetracene Fluorescence by Hydrogen-Bonded Phenol-Base Pairs
    • Biczok, L.; Linschitz, H. Concerted Electron and Proton Movement in Quenching of Triplet C60 and Tetracene Fluorescence by Hydrogen-Bonded Phenol-Base Pairs J. Phys. Chem. 1995, 99, 1843-1845
    • (1995) J. Phys. Chem. , vol.99 , pp. 1843-1845
    • Biczok, L.1    Linschitz, H.2
  • 29
    • 0035857089 scopus 로고    scopus 로고
    • +. cation radical
    • DOI 10.1021/jp012778s
    • Biczok, L.; Linschitz, H. Oxidation of Triplet C60 by Hydrogen-Bonded Chloranil: Efficient Formation, Spectrum and Charge-Shift Reactions of C60+. Cation Radical J. Phys. Chem. A 2001, 105, 11051-11056 (Pubitemid 35378594)
    • (2001) Journal of Physical Chemistry A , vol.105 , Issue.49 , pp. 11051-11056
    • Biczok, L.1    Linschitz, H.2
  • 30
    • 34247636738 scopus 로고    scopus 로고
    • The role of acids and bases on the electrochemical oxidation of hydroquinone: Hydrogen bonding interactions in acetonitrile
    • DOI 10.1016/j.jelechem.2007.02.031, PII S0022072807001155
    • Astudillo, P. D.; Tiburcio, J.; Gozalez, F. J. The role of acids and bases on the electrochemical oxidation of hydroquinone: Hydrogen bonding interactions in acetonitrile J. Electroanal. Chem. 2007, 604, 57-64 (Pubitemid 46671589)
    • (2007) Journal of Electroanalytical Chemistry , vol.604 , Issue.1 , pp. 57-64
    • Astudillo, P.D.1    Tiburcio, J.2    Gonzalez, F.J.3
  • 31
    • 0346937281 scopus 로고    scopus 로고
    • Theoretical and Electrochemical Study of Quinone-Benzoic Acid Adduct Linked by Hydrogen Bonds
    • Garza, J.; Vargas, R.; Gomez, M.; Gonzalez, I.; Gonzalez, F. J. Theoretical and Electrochemical Study of Quinone-Benzoic Acid Adduct Linked by Hydrogen Bonds J. Phys. Chem. A 2003, 107, 11161-11168
    • (2003) J. Phys. Chem. A , vol.107 , pp. 11161-11168
    • Garza, J.1    Vargas, R.2    Gomez, M.3    Gonzalez, I.4    Gonzalez, F.J.5
  • 32
    • 24744438878 scopus 로고    scopus 로고
    • Electrochemical approach to concerted proton and electron transfers. Reduction of the water-superoxide ion complex
    • DOI 10.1021/ja053911n
    • Costentin, C.; Evans, D. H.; Robert, M.; Saveant, J.-M.; Singh, P. S. Electrochemical Approach to Concerted Proton and Electron Transfers. Reduction of the Water-Superoxide Ion Complex J. Am. Chem. Soc. 2005, 127, 12490-12491 (Pubitemid 41292158)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.36 , pp. 12490-12491
    • Costentin, C.1    Evans, D.H.2    Robert, M.3    Saveant, J.-M.4    Singh, P.S.5
  • 33
    • 33847700875 scopus 로고    scopus 로고
    • Electrochemical concerted proton and electron transfers. Further insights in the reduction mechanism of superoxide ion in the presence of water and other weak acids
    • DOI 10.1021/jp068322y
    • Saveant, J.-M. Electrochemical Concerted Proton and Electron Transfers. Further Insights in the Reduction Mechanism of Superoxide Ion in the Presence of Water and Other Weak Acids J. Phys. Chem. C 2007, 111, 2819-2822 (Pubitemid 46384286)
    • (2007) Journal of Physical Chemistry C , vol.111 , Issue.7 , pp. 2819-2822
    • Saveant, J.-M.1
  • 34
    • 33646069041 scopus 로고    scopus 로고
    • Electrochemical and Homogeneous Proton-Coupled Electron Transfers: Concerted Pathways in the One-Electron Oxidation of a Phenol Coupled with and Intramolecular Amine-Driven Proton Transfer
    • Costentin, C.; Robert, M.; Saveant, J.-M. Electrochemical and Homogeneous Proton-Coupled Electron Transfers: Concerted Pathways in the One-Electron Oxidation of a Phenol Coupled with and Intramolecular Amine-Driven Proton Transfer J. Am. Chem. Soc. 2006, 128, 4552-4553
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 4552-4553
    • Costentin, C.1    Robert, M.2    Saveant, J.-M.3
  • 35
    • 84975363015 scopus 로고
    • Proton Effects in the Electrochemistry of the Quinone Hydroquinone System in Aprotic Solvents
    • Eggins, B. R.; Chambers, J. Q. Proton Effects in the Electrochemistry of the Quinone Hydroquinone System in Aprotic Solvents J. Electrochem. Soc. 1970, 117, 186-192
    • (1970) J. Electrochem. Soc. , vol.117 , pp. 186-192
    • Eggins, B.R.1    Chambers, J.Q.2
  • 36
    • 2042540105 scopus 로고
    • The Hydroquinone-QuinoneRedox Behaviour in Acetonitrile
    • Parker, V. D. The Hydroquinone-QuinoneRedox Behaviour in Acetonitrile Chem. Commun. 1969, 716-717
    • (1969) Chem. Commun. , pp. 716-717
    • Parker, V.D.1
  • 37
    • 0000002977 scopus 로고
    • The Anodic Oxidation of Hydroquinone in Acetonitrile on the Question of a Possible One Electron Intermediate
    • Parker, V. D. The Anodic Oxidation of Hydroquinone in Acetonitrile on the Question of a Possible One Electron Intermediate Electrochim. Acta 1973, 18, 519-524
    • (1973) Electrochim. Acta , vol.18 , pp. 519-524
    • Parker, V.D.1
  • 39
    • 0000678798 scopus 로고
    • Recommendations on reporting electrode potentials in nonaqueous solvents: IUPC commision on electrochemistry
    • Gritzner, G.; Kuta, J. Recommendations on reporting electrode potentials in nonaqueous solvents: IUPC commision on electrochemistry Electrochim. Acta 1984, 29, 869-873
    • (1984) Electrochim. Acta , vol.29 , pp. 869-873
    • Gritzner, G.1    Kuta, J.2
  • 40
    • 33646376290 scopus 로고
    • Spin Diffusion Measurements: Spin Echoes in the Presence of a Time-Dependent Field Gradient
    • Stejskal, E. O.; Tanner, J. E. Spin Diffusion Measurements: Spin Echoes in the Presence of a Time-Dependent Field Gradient J. Chem. Phys. 1965, 42, 288-292
    • (1965) J. Chem. Phys. , vol.42 , pp. 288-292
    • Stejskal, E.O.1    Tanner, J.E.2
  • 42
    • 13244253788 scopus 로고    scopus 로고
    • Diffusion NMR spectroscopy in supramolecular and combinatorial chemistry: An old parameter - New insights
    • DOI 10.1002/anie.200300637
    • Cohen, Y.; Avram, L.; Frish, L. Diffusion NMR Spectroscopy in Supramolecular and Combinatorial Chemistry: An Old Parameter-New Insights Angew. Chem., Int. Ed. Engl. 2005, 44, 520-554 (Pubitemid 40192558)
    • (2005) Angewandte Chemie - International Edition , vol.44 , Issue.4 , pp. 520-554
    • Cohen, Y.1    Avram, L.2    Frish, L.3
  • 43
    • 33645822272 scopus 로고    scopus 로고
    • A Simple Method Based on NMR Spectroscopy and Ultramicroelectrode Volatmmetry for the Determination of the Number of Electrons in Faradic Processes
    • Sun, H.; Chen, W.; Kaifer, A. E. A Simple Method Based on NMR Spectroscopy and Ultramicroelectrode Volatmmetry for the Determination of the Number of Electrons in Faradic Processes Organometallics 2006, 25, 1828-1830
    • (2006) Organometallics , vol.25 , pp. 1828-1830
    • Sun, H.1    Chen, W.2    Kaifer, A.E.3
  • 44
    • 33947482378 scopus 로고
    • Hydrogen Bonding in Fluoro Alcohols
    • Middleton, W. J.; Lindsey, R. V. Hydrogen Bonding in Fluoro Alcohols J. Am. Chem. Soc. 1964, 86, 4948-4952
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 4948-4952
    • Middleton, W.J.1    Lindsey, R.V.2
  • 48
    • 0029926948 scopus 로고    scopus 로고
    • The energetics of hydrogen bonds in model systems: Implications for enzymatic catalysis
    • Shan, S.; Loh, S.; Herschlag, D. The Energetics of Hydrogen Bonds in Model Systems: Implications for Enzymatic Catalysis Science 1996, 272, 97-101 (Pubitemid 26110758)
    • (1996) Science , vol.272 , Issue.5258 , pp. 97-101
    • Shan, S.-O.1    Loh, S.2    Herschlag, D.3
  • 49
    • 0000064714 scopus 로고
    • Redox Chemistry of Metal-Catechol Complexes in Aprotic Media. 1. Electrochemistry of Substituted Catechols and Their Oxidation Products
    • Stallings, M. D.; Morrison, M. M.; Sawyer, D. T. Redox Chemistry of Metal-Catechol Complexes in Aprotic Media. 1. Electrochemistry of Substituted Catechols and Their Oxidation Products Inorg. Chem. 1981, 20, 2655-2660
    • (1981) Inorg. Chem. , vol.20 , pp. 2655-2660
    • Stallings, M.D.1    Morrison, M.M.2    Sawyer, D.T.3
  • 50
    • 84991970866 scopus 로고
    • Electrochemistry of Quinones
    • Eds.; John Wiley and Sons: New York,; Vol
    • Chambers, J. Q. Electrochemistry of Quinones. In The Chemistry of Quinoid Compounds; Patai, S.; Rappoport, Z., Eds.; John Wiley and Sons: New York, 1988; Vol. 2, pp 719-758.
    • (1988) The Chemistry of Quinoid Compounds , vol.2 , pp. 719-758
    • Chambers, J.Q.1    Patai, S.2    Rappoport, Z.3
  • 51
    • 0347424625 scopus 로고
    • The Oxidation of Hydroquinone by Protonated Quinone
    • Hammerich, O.; Parker, V. D. The Oxidation of Hydroquinone by Protonated Quinone Acta Chem. Scand., Ser. B 1982, 36, 63-64
    • (1982) Acta Chem. Scand., Ser. B , vol.36 , pp. 63-64
    • Hammerich, O.1    Parker, V.D.2
  • 53
    • 11544291734 scopus 로고
    • Disproportionation of Quinone Radical Anions in Protic Solvents at High pH
    • Wipf, D. O.; Wehmeyer, K. R.; Wightman, R. M. Disproportionation of Quinone Radical Anions in Protic Solvents at High pH J. Org. Chem. 1986, 51, 4760-4764
    • (1986) J. Org. Chem. , vol.51 , pp. 4760-4764
    • Wipf, D.O.1    Wehmeyer, K.R.2    Wightman, R.M.3
  • 54
    • 0033562403 scopus 로고    scopus 로고
    • Effect of comproportionation on voltammograms for two-electron reactions with an irreversible second electron transfer
    • DOI 10.1021/ac990066g
    • Lehmann, M. W.; Evans, D. H. Effect of Comproportionation on Voltammograms for Two-Electron Reactions with an Irreversible Second Electron Transfer Anal. Chem. 1999, 71, 1947-1950 (Pubitemid 29233155)
    • (1999) Analytical Chemistry , vol.71 , Issue.10 , pp. 1947-1950
    • Lehmann, M.W.1    Evans, D.H.2
  • 55
    • 0002451602 scopus 로고
    • Electrochemical Reactions with Protonations at Equilibrium. Part II. The 1 e-, 1 H+ Reaction (Four-Member Square Scheme) for a Heterogeneous Reaction
    • Laviron, E. Electrochemical Reactions with Protonations at Equilibrium. Part II. The 1 e-, 1 H+ Reaction (Four-Member Square Scheme) for a Heterogeneous Reaction J. Electroanal. Chem. 1981, 124, 1-7
    • (1981) J. Electroanal. Chem. , vol.124 , pp. 1-7
    • Laviron, E.1
  • 56
    • 0011300312 scopus 로고
    • Electrochemical Reactions with Protonations at Equilibrium. Part III. The 1 e-, 2 H+ Reaction (Six-Member Ladder Scheme) for a Surface or for a Heterogenous Reaction
    • Laviron, E. Electrochemical Reactions with Protonations at Equilibrium. Part III. The 1 e-, 2 H+ Reaction (Six-Member Ladder Scheme) for a Surface or for a Heterogenous Reaction J. Electroanal. Chem. 1981, 124, 9-17
    • (1981) J. Electroanal. Chem. , vol.124 , pp. 9-17
    • Laviron, E.1
  • 57
    • 0021097438 scopus 로고
    • Electrochemical Reactions with Protonations at Equilibrium. Part VII. The 2 e-, 1 H+ Reaction (Six-Member fence scheme) for a Surface or for a Heterogeneous Reaction in the Absence of Disproportionation or Dimerization
    • Laviron, E. Electrochemical Reactions with Protonations at Equilibrium. Part VII. The 2 e-, 1 H+ Reaction (Six-Member fence scheme) for a Surface or for a Heterogeneous Reaction in the Absence of Disproportionation or Dimerization J. Electroanal. Chem. 1983, 146, 1-13 (Pubitemid 14468753)
    • (1983) Journal of electroanalytical chemistry and interfacial electrochemistry , vol.146 , Issue.1 , pp. 1-13
    • Laviron, E.1
  • 58
    • 0021097430 scopus 로고
    • Electrochemical Reactions with Protonations at Equilibrium. Part VIII. The 2 e-, 2 H+ Reaction (Nine-Member Square Scheme) for a Surface or for a Heterogeneous Reaction in the Absence of Disproportionation and Dimerization Reactions
    • Laviron, E. Electrochemical Reactions with Protonations at Equilibrium. Part VIII. The 2 e-, 2 H+ Reaction (Nine-Member Square Scheme) for a Surface or for a Heterogeneous Reaction in the Absence of Disproportionation and Dimerization Reactions J. Electroanal. Chem. 1983, 146, 15-36 (Pubitemid 14468754)
    • (1983) Journal of electroanalytical chemistry and interfacial electrochemistry , vol.146 , Issue.1 , pp. 15-36
    • Laviron, E.1
  • 59
    • 0021408999 scopus 로고
    • Electrochemical Reactions with Protonations at Equilibrium. Part X. The Kinetics of the p-Benzoquinone/Hydroquinone Couple on a Platinum Electrode
    • Laviron, E. Electrochemical Reactions with Protonations at Equilibrium. Part X. The Kinetics of the p-Benzoquinone/Hydroquinone Couple on a Platinum Electrode J. Electroanal. Chem. 1984, 164, 213-227 (Pubitemid 14589347)
    • (1984) Journal of electroanalytical chemistry and interfacial electrochemistry , vol.164 , Issue.2 , pp. 213-227
    • Laviron, E.1
  • 60
    • 35449008481 scopus 로고    scopus 로고
    • Voltammetry of quinones in unbuffered aqueous solution: Reassessing the roles of proton transfer and hydrogen bonding in the aqueous electrochemistry of quinones
    • DOI 10.1021/ja0743083
    • Quan, M.; Sanchez, D.; Wasylkiw, M. F.; Smith, D. K. Voltammetry of Quinones in Unbuffered Aqueous Solution: Reassessing the Roles of Proton Transfer and Hydrogen Bonding in the Aqueous Electrochemistry of Quinones J. Am. Chem. Soc. 2007, 129, 12847-12856 (Pubitemid 350004497)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.42 , pp. 12847-12856
    • Quan, M.1    Sanchez, D.2    Wasylkiw, M.F.3    Smith, D.K.4
  • 61
    • 0008848909 scopus 로고
    • Linear Sweep Voltammetry: Kinetic Control by Charge Transfer and/or Secondary Chemical Reactions
    • Nadjo, L.; Saveant, J.-M. Linear Sweep Voltammetry: Kinetic Control by Charge Transfer and/or Secondary Chemical Reactions J. Electroanal. Chem. 1973, 48, 113-145
    • (1973) J. Electroanal. Chem. , vol.48 , pp. 113-145
    • Nadjo, L.1    Saveant, J.-M.2
  • 63
    • 35449001112 scopus 로고    scopus 로고
    • Electron Transfer, Bond Breaking and Bond Formation
    • Ed.; Academic Press: New York,; Vol
    • Saveant, J.-M. Electron Transfer, Bond Breaking and Bond Formation. In Advances in Physical Organic Chemistry; Tidwell, T. T., Ed.; Academic Press: New York, 2000; Vol. 35, pp 117-192.
    • (2000) Advances in Physical Organic Chemistry , vol.35 , pp. 117-192
    • Saveant, J.-M.1    Tidwell, T.T.2
  • 64
    • 0042020301 scopus 로고    scopus 로고
    • Adsorption of Quaternary Pyridinium Compounds at Pt Electrodes in Neutral and Weakly Alkaline Solutions
    • Birss, V.; Dang, K.; Wong, J. E.; Wong, R. P. C. Adsorption of Quaternary Pyridinium Compounds at Pt Electrodes in Neutral and Weakly Alkaline Solutions J. Electroanal. Chem. 2003, 550-551, 67-79
    • (2003) J. Electroanal. Chem. , vol.550-551 , pp. 67-79
    • Birss, V.1    Dang, K.2    Wong, J.E.3    Wong, R.P.C.4
  • 66
    • 0035857429 scopus 로고    scopus 로고
    • Proton-coupled electron transfer in duplex DNA: Driving force dependence and isotope effects on electrocatalytic oxidation of guanine [4]
    • DOI 10.1021/ja003788u
    • Weatherly, S. C.; Yang, I. V.; Thorp, H. H. Proton-Coupled Electron Transfer in Duplex DNA: Driving Force Dependence and Isotope Effects on Electrocatalytic Oxidation of Guanine J. Am. Chem. Soc. 2001, 123, 1236-1237 (Pubitemid 32148190)
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.6 , pp. 1236-1237
    • Weatherly, S.C.1    Yang, I.V.2    Thorp, H.H.3
  • 68
    • 15744375592 scopus 로고    scopus 로고
    • Switching the redox mechanism: Models for proton-coupled electron transfer from tyrosine and tryptophan
    • DOI 10.1021/ja044395o
    • Sjodin, M.; Styring, S.; Wolpher, H.; Xu, W.; Sun, L.; Hammarstrom, L. Switching the Redox Mechanism: Models for Proton-Coupled Electron Transfer from Tyrosine and Tryptophan J. Am. Chem. Soc. 2005, 127, 3855-3863 (Pubitemid 40411426)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.11 , pp. 3855-3863
    • Sjodin, M.1    Styring, S.2    Wolpher, H.3    Xu, Y.4    Sun, L.5    Hammarstrom, L.6
  • 69
    • 5644228648 scopus 로고    scopus 로고
    • One-electron oxidation of a hydrogen-bonded phenol occurs by concerted proton-coupled electron transfer
    • Rhile, I. J.; Mayer, J. M. One-Electron Oxidation of Hydrogen-Bonded Phenol Occurs by Concerted Proton-Coupled Electron Transfer J. Am. Chem. Soc. 2004, 126, 12718-12719 (Pubitemid 39372269)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.40 , pp. 12718-12719
    • Rhile, I.J.1    Mayer, J.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.