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"Front Matter". In: Organosilanes in Radical Chemistry - Index of

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226 <strong>In</strong>dex<br />

Triethylsilane<br />

as mediator with monosubstituted<br />

alkene 153<br />

reduc<strong>in</strong>g agent 70–71<br />

Si w H dissociation enthalpy 22t<br />

with am<strong>in</strong>yl 39t<br />

with aroyloxyl 42<br />

with benzophenone triplet 44t<br />

with cumylperoxyl 40t<br />

with perfluoroalkyl 36t<br />

with primary alkyl 33t<br />

with [1.1.1]propellane 97<br />

with tert-butoxyl 40t<br />

with tertiary alkyl 36t<br />

with thiocarbonyl derivatives 71<br />

with thiyl 42, 43t<br />

Triethylsilyl radical<br />

addition to alkene 89, 89t<br />

addition to alkyne 98<br />

with alkyl bromide 72t<br />

with alkyl chloride 72t<br />

with alkyl iodide 72t<br />

addition to carbon-nitrogen double<br />

bond 108,109t<br />

addition to carbonyl compound 100,<br />

101, 102t<br />

with polyhalogenated compound 72t<br />

with sulfonyl halide 73<br />

addition to term<strong>in</strong>al alkene 153<br />

Trimethylsilane<br />

enthalpy <strong>of</strong> formation 21t<br />

gas-phase acidity 27t<br />

gas-phase basicity 28t<br />

Si w H dissociation enthalpy 21t<br />

Trimethylsilyl radical<br />

addition to alkene 88, 89, 90<br />

addition to cumulene and heterocumulene<br />

109t, 110<br />

electron aff<strong>in</strong>ity 27t<br />

enthalpy <strong>of</strong> formation 21, 21t, 24<br />

ionization potential 28t<br />

self-term<strong>in</strong>ation 51<br />

Triphenylsilane<br />

with am<strong>in</strong>yl 39t<br />

with cumylperoxyl 40t<br />

methylenelactone 95<br />

with monosubstituted acetylene 98<br />

with phenyl 36t<br />

with primary alkyl 33t<br />

with tert-butoxyl 40t<br />

tertiary alkyl 36t<br />

with thiyl 42, 43t<br />

Triphenylsilyl radical with alkyl<br />

chloride 74t<br />

Triphenylt<strong>in</strong> hydride 125, 126, 131, 136<br />

Triqu<strong>in</strong>ane 151, 179<br />

Tris(methylthio)silane<br />

reduc<strong>in</strong>g agent 78<br />

Si w H dissociation enthalpy 22t<br />

Tris(trimethylsilyl)silane<br />

autoxidation 190, 191, 192, 192s<br />

gas-phase acidity 27t<br />

reduc<strong>in</strong>g agent 53–54, 57<br />

Si w H dissociation enthalpy 22t<br />

with acyl radical 36t<br />

with acid chloride 58<br />

with aldehyde 105<br />

with alkyl chloride 57, 58<br />

with alkyl bromide 55, 56<br />

with alkyl iodide 55<br />

with alkyl isocyanide 67<br />

with alkyl selenide 60<br />

with alkyl sulfide 59, 60<br />

with allyl phenyl sulfide 96<br />

with am<strong>in</strong>yl radical 39t<br />

with aryloxyl radical 41<br />

with benzophenone triplet 44t<br />

with a-chiral disubstituted olef<strong>in</strong> 94<br />

with cumylperoxyl radical 40t<br />

with dialkyl ketone 102, 103<br />

with diethyl methyl fumarate 93<br />

with disubstituted acetylene 99<br />

with gem-dichloride 58<br />

with gem-disubstituted olef<strong>in</strong> 92<br />

with methylmaleic anhydride 93<br />

with monosubstituted acetylene 98, 99<br />

with monosubstituted olef<strong>in</strong> 92<br />

with nitro derivatives 68<br />

with nitroxide 67<br />

with oxygen 70, 193<br />

with perfluoroalkyl radical 36t<br />

with peroxyl radical 193,<br />

with phenyl radical 36t<br />

with phenyl selenoester 61

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