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Journal Abstract Search

453 related items for PubMed ID: 19281146

  • 21. Addition reactions of alkyl and carboxyl radicals to vinylidene fluoride.
    Hirunsit P, Balbuena PB.
    J Phys Chem A; 2008 May 15; 112(19):4483-9. PubMed ID: 18396852
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  • 25. Thermochemistry and reaction paths in the oxidation reaction of benzoyl radical: C6H5C•(═O).
    Sebbar N, Bozzelli JW, Bockhorn H.
    J Phys Chem A; 2011 Oct 27; 115(42):11897-914. PubMed ID: 21942384
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  • 26. Electron super-rich radicals in the gas phase. A neutralization-reionization mass spectrometric and ab initio/RRKM study of diaminohydroxymethyl and triaminomethyl radicals.
    Hao C, Seymour JL, Turecek F.
    J Phys Chem A; 2007 Sep 13; 111(36):8829-43. PubMed ID: 17705355
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  • 27. Rate constants for reactions of alkyl radicals with water and methanol complexes of triethylborane.
    Jin J, Newcomb M.
    J Org Chem; 2007 Jul 06; 72(14):5098-103. PubMed ID: 17579450
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  • 30. Hydrogen-atom transfer in reactions of organic radicals with [Co(II)(por)]* (por = porphyrinato) and in subsequent addition of [Co(H)(por)] to olefins.
    de Bruin B, Dzik WI, Li S, Wayland BB.
    Chemistry; 2009 Jul 06; 15(17):4312-20. PubMed ID: 19266521
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  • 32. Photoion photoelectron coincidence spectroscopy of primary amines RCH2NH2 (R = H, CH3, C2H5, C3H7, i-C3H7): alkylamine and alkyl radical heats of formation by isodesmic reaction networks.
    Bodi A, Kercher JP, Bond C, Meteesatien P, Sztáray B, Baer T.
    J Phys Chem A; 2006 Dec 21; 110(50):13425-33. PubMed ID: 17165868
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  • 35. An ab-initio study of some homolytic substitution reactions of acyl radicals at silicon, germanium and tint.
    Matsubara H, Schiesser CH.
    Org Biomol Chem; 2003 Dec 07; 1(23):4335-41. PubMed ID: 14685338
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  • 38. Ab initio G3-type/statistical theory study of the formation of indene in combustion flames. I. Pathways involving benzene and phenyl radical.
    Kislov VV, Mebel AM.
    J Phys Chem A; 2007 May 17; 111(19):3922-31. PubMed ID: 17260977
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  • 40. Activation energies of pericyclic reactions: performance of DFT, MP2, and CBS-QB3 methods for the prediction of activation barriers and reaction energetics of 1,3-dipolar cycloadditions, and revised activation enthalpies for a standard set of hydrocarbon pericyclic reactions.
    Ess DH, Houk KN.
    J Phys Chem A; 2005 Oct 27; 109(42):9542-53. PubMed ID: 16866406
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