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Tert-dodecanethiol

A-DODECAL CTONE see DXS700 A-DODECALACTONE see HBP450 1-DODECANAL see DXTOOO 1-DODECANMIIN E (9CI) see DXNX OOO 1-DODECANETHIOL see LBXOOO tert-DODECANETHIOL see DXT800 DODECANOIC ACID see LBLOOO DODECANOIC ACID, CADNDUM SALT (9CI) see CAG775... [Pg.1661]

Monodisperse wurtzite CuInxGai xS2 (GIGS) nanocrystals have been synthesized from metal-acetylacetonate complexes and a mixture of sulfur sources as 1-dodecanethiol and tert-dodecanethiol. The morphology of the nanocrystals can be controlled in the form of bullet-like, rod-like, and tadpole-like shapes. The band gap of the nanocrystals increased with the increase in gallium concentration. [Pg.33]

Beilstein Handbook Reference) BRN 1738382 CCRIS 6030 t-DDM t-Dodecanethiol tert-Dodeoyi mercaptan terc.Dodecylmerkaptan tert-Dodeoanethiol tert-Dodecylthiol EINECS 246-619-1 2,3,3,4,4,5-Hexamethyl-2-hexanethiol Sulfole 120,... [Pg.253]

HI = hot-injection method, HU = heating-up method, RT = room temperature, CdMe = dimethyl cadmium, ZnEt = diethylzinc, TMS = trimethlsilyl, (BDMSj Te = his tert-butyldimethylsilyljteUuride, TDPA = tetradecylphosphonic acid, ODPA = octadecy-Iphosphonic acid, SA = stearic acid, LA = lauric acid, MA = myristic acid, OA = oleic acid, ac = acetate, acac = acetylacetonate, st = stearate, hdx = hexadecylxanthate, ex = ethylxanthate, dx = decylxanthate, TOPO = trioctylphosphine, HDA = hexadecylamine, DDA = dodecylamine, ODA = octadecylamine, TOP = trioctylphosphine, TBP = tribu-tylphosphine, ODE = 1-octadecene, HH = hexadecylhexadecanoate, BP = benzophenone, TOA = trioctylamine, OAm = oleylamine, DPE = diphenylether, TAA = thioacetamide TEA = triethanolamine, DDT = dodecanethiol, dedc= diethyldithiocarbamate. [Pg.173]

Thiobis(2-methyl-6-butylphenol) Thiodiethylene bis(3,5-di-tert-butyl-4-hydroxycinnamate) 4,6-Bis(octylthiomethyl)-o-cresol Reaction product of nonylphenol, dodecanethiol, and formaldehyde... [Pg.628]

Hydrogen-transfer Reagent in Radical Reactions. Thiols, in particular tertiary mercaptans such as tert-butanethiol and triethylmethanethiol, have been widely used in radical reactions to trap radical intermediates by hydrogen atom transfer. ferf-Dodecanethiol is a vahd substitute for those mercaptans, since it is cheap, relatively odorless compared to the other alkanethiols, and generally equally efficient with respect to the hydrogen donor properties. [Pg.270]

Large quantities of CuInSe2 nanocrystals were synthesised by the reaction of copper iodide, indium acetate and tert-butylphosphine selenide in a mixture of dodecanethiol, octadecene, oleic acid at 200 °C. The nanocrystals produced showed tunable photoluminescence spectra ranging from 600 to 850nm. Two-dimensional photoluminescence spectra are also reported with the synthesis of Type-I heterostructured CuInSe2/ZnS nanocrystals. [Pg.31]


See other pages where Tert-dodecanethiol is mentioned: [Pg.341]    [Pg.79]    [Pg.341]    [Pg.95]    [Pg.102]    [Pg.112]    [Pg.578]    [Pg.120]    [Pg.598]    [Pg.253]    [Pg.711]    [Pg.746]    [Pg.269]    [Pg.270]    [Pg.271]    [Pg.271]    [Pg.656]    [Pg.32]    [Pg.341]    [Pg.79]    [Pg.341]    [Pg.95]    [Pg.102]    [Pg.112]    [Pg.578]    [Pg.120]    [Pg.598]    [Pg.253]    [Pg.711]    [Pg.746]    [Pg.269]    [Pg.270]    [Pg.271]    [Pg.271]    [Pg.656]    [Pg.32]    [Pg.47]    [Pg.72]    [Pg.73]    [Pg.680]    [Pg.319]    [Pg.383]    [Pg.46]    [Pg.47]    [Pg.215]    [Pg.223]   
See also in sourсe #XX -- [ Pg.136 ]




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Dodecanethiol

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