Hydrogen atom abstraction reactions independent of C–H bond dissociation energies of organic substrates in water: significance of oxidant–substrate adduct formation

Tomoya Ishizuka; Shingo Ohzu; Hiroaki Kotani; Yoshihito Shiota; Kazunari Yoshizawa; Takahiko Kojima

doi:10.1039/c3sc53002g

Hydrogen atom abstraction reactions independent of C–H bond dissociation energies of organic substrates in water: significance of oxidant–substrate adduct formation

Chemical Science ◽

10.1039/c3sc53002g ◽

2014 ◽

Vol 5 (4) ◽

pp. 1429-1436 ◽

Cited By ~ 19

Author(s):

Tomoya Ishizuka ◽

Shingo Ohzu ◽

Hiroaki Kotani ◽

Yoshihito Shiota ◽

Kazunari Yoshizawa ◽

...

Keyword(s):

Hydrogen Bonding ◽

Hydrogen Atom ◽

Transition States ◽

Adduct Formation ◽

Hydrogen Atom Abstraction ◽

Organic Substrates ◽

Bond Dissociation Energies ◽

Bond Dissociation ◽

Dissociation Energies ◽

Oxo Complexes

Adduct formation between Ru(iv)–oxo complexes and substrates with hydrogen bonding affords condensed transition states for substrate oxidations in water.

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Hydrogen Atom Transfer Reactions of C2-, C4-, and C6-: Bond Dissociation Energies of Linear H−C2n-and H−C2n(n= 1, 2, 3)

The Journal of Physical Chemistry A ◽

10.1021/jp077181c ◽

2008 ◽

Vol 112 (6) ◽

pp. 1261-1267 ◽

Cited By ~ 3

Author(s):

Yang Shi ◽

Kent M. Ervin

Keyword(s):

Hydrogen Atom ◽

Hydrogen Atom Transfer ◽

Transfer Reactions ◽

Atom Transfer ◽

Bond Dissociation Energies ◽

Bond Dissociation ◽

Dissociation Energies ◽

Atom Transfer Reactions

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Transition from Hydrogen Atom to Hydride Abstraction by Mn4O4(O2PPh2)6versus [Mn4O4(O2PPh2)6]+: O−H Bond Dissociation Energies and the Formation of Mn4O3(OH)(O2PPh2)6

Inorganic Chemistry ◽

10.1021/ic025977e ◽

2003 ◽

Vol 42 (9) ◽

pp. 2849-2858 ◽

Cited By ~ 28

Author(s):

Thomas G. Carrell ◽

Emilie Bourles ◽

Matthew Lin ◽

G. Charles Dismukes

Keyword(s):

Hydrogen Atom ◽

Bond Dissociation Energies ◽

Bond Dissociation ◽

Dissociation Energies ◽

Hydride Abstraction

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ChemInform Abstract: POLAR EFFECTS IN RADICAL REACTIONS. 6. THE SEPARATION OF SUBSTITUENT EFFECTS ON TRANSITION STATES FROM SUBSTITUENT EFFECTS ON BOND DISSOCIATION ENERGIES. ABSTRACTION OF IODINE FROM SUBSTITUTED IODOBENZENES BY P-NITROPHENYL RADICALS

Chemischer Informationsdienst ◽

10.1002/chin.197720107 ◽

1977 ◽

Vol 8 (20) ◽

pp. no-no

Author(s):

W. H. JUN. DAVIS ◽

J. H. GLEATON ◽

W. A. PRYOR

Keyword(s):

Transition States ◽

Substituent Effects ◽

Radical Reactions ◽

Bond Dissociation Energies ◽

Bond Dissociation ◽

Dissociation Energies

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Heterolytic and homolytic C-D bond dissociation energies of NADH models in acetonitrile and primary isotopic effects on hydride versus hydrogen atom transfer reactions

Science China Chemistry ◽

10.1007/s11426-012-4679-6 ◽

2012 ◽

Vol 55 (10) ◽

pp. 2054-2056 ◽

Cited By ~ 1

Author(s):

ChaoTun Cao ◽

Yue Tan ◽

Xiao-Qing Zhu

Keyword(s):

Hydrogen Atom ◽

Hydrogen Atom Transfer ◽

Transfer Reactions ◽

Atom Transfer ◽

Bond Dissociation Energies ◽

Bond Dissociation ◽

Dissociation Energies ◽

Atom Transfer Reactions ◽

Isotopic Effects

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Bond Dissociation Energies and Equilibrium Structures of Cu+(MeOH)x,x= 1−6, in the Gas Phase: Competition between Solvation of the Metal Ion and Hydrogen-Bonding Interactions

The Journal of Physical Chemistry A ◽

10.1021/jp076964v ◽

2008 ◽

Vol 112 (3) ◽

pp. 388-401 ◽

Cited By ~ 12

Author(s):

Z. Yang ◽

N. S. Rannulu ◽

Y. Chu ◽

M. T. Rodgers

Keyword(s):

Hydrogen Bonding ◽

Gas Phase ◽

Metal Ion ◽

Bond Dissociation Energies ◽

Phase Competition ◽

Bond Dissociation ◽

Dissociation Energies ◽

Hydrogen Bonding Interactions ◽

Equilibrium Structures

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Polar effects in radical reactions. 6. The separation of substituent effects on transition states from substituent effects on bond dissociation energies. Abstraction of iodine from substituted iodobenzenes by p-nitrophenyl radicals

The Journal of Organic Chemistry ◽

10.1021/jo00421a002 ◽

1977 ◽

Vol 42 (1) ◽

pp. 7-12 ◽

Cited By ~ 19

Author(s):

William H. Davis ◽

John H. Gleaton ◽

William A. Pryor

Keyword(s):

Transition States ◽

Substituent Effects ◽

Radical Reactions ◽

Bond Dissociation Energies ◽

Bond Dissociation ◽

Dissociation Energies

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Heterolytic and homolytic C-D bond dissociation energies of NADH models in acetonitrile and primary isotopic effects on hydride versus hydrogen atom transfer reactions

Scientia Sinica Chimica ◽

10.1360/zb2012-42-10-1491 ◽

2012 ◽

Vol 42 (10) ◽

pp. 1491-1492

Author(s):

Yue TAN ◽

Xiao-Qing ZHU ◽

ChaoTun CAO

Keyword(s):

Hydrogen Atom ◽

Hydrogen Atom Transfer ◽

Transfer Reactions ◽

Atom Transfer ◽

Bond Dissociation Energies ◽

Bond Dissociation ◽

Dissociation Energies ◽

Atom Transfer Reactions ◽

Isotopic Effects

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Kinetic study of the reaction of benzoyl peroxide with phenolic compounds. A technique for the evaluation of phenolic O-H bond dissociation energies

Journal de Chimie Physique ◽

10.1051/jcp/1989862057 ◽

1989 ◽

Vol 86 ◽

pp. 2057-2066 ◽

Cited By ~ 2

Author(s):

Claire Rousseau-Richard ◽

Claude Richard ◽

René Martin

Keyword(s):

Phenolic Compounds ◽

Kinetic Study ◽

Benzoyl Peroxide ◽

Bond Dissociation Energies ◽

Bond Dissociation ◽

Dissociation Energies

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Experimental bond dissociation energies of benzylpyridinium thermometer ions determined by threshold-CID and RRKM modeling

International Journal of Mass Spectrometry ◽

10.1016/j.ijms.2017.03.002 ◽

2017 ◽

Vol 417 ◽

pp. 69-75 ◽

Cited By ~ 9

Author(s):

David Gatineau ◽

Antony Memboeuf ◽

Anne Milet ◽

Richard B. Cole ◽

Héloïse Dossmann ◽

...

Keyword(s):

Bond Dissociation Energies ◽

Bond Dissociation ◽

Dissociation Energies ◽

Thermometer Ions

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Electron affinities of a homologous series of tertiary alkyl radicals and their C–H bond dissociation energies (BDEs)

Tetrahedron ◽

10.1016/j.tet.2008.12.043 ◽

2009 ◽

Vol 65 (8) ◽

pp. 1655-1659 ◽

Cited By ~ 2

Author(s):

Panayiotis S. Petrou ◽

Athanassios V. Nicolaides

Keyword(s):

Homologous Series ◽

Bond Dissociation Energies ◽

Electron Affinities ◽

Alkyl Radicals ◽

Bond Dissociation ◽

Dissociation Energies ◽

Tertiary Alkyl

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