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Tetrabutylammonium tetrakis borate

FIG. 6 Typical cyclic voltammogram obtained for the transfer of pilocarpine hydrochloride at the water-DCE interface. The organic phase contains 0.01 M tetrabutylammonium tetrakis(4-chloro-phenyl)borate, the aqueous solution is 0.01 M HCl + 0.2 mM pilocarpine hydrochloride, and the sweep rate is fixed at 10, 25, 75, 100, and 150mV/s. (Reprinted from Ref. 229.)... [Pg.741]

Tetrabutylammonium tetrakis(iiiethyl-thiomethyl)borate(l-). See 1-Butan-aminium, AWA tributyl-, tetrakis-[(methylthio)methyl]borate(l-), [158310-79-3]... [Pg.320]

Suitable electrolytes for the aqueous phase (w) comprise, for example, LiCl, HCl, MgCl2, MgS04, while suitable electrolytes for the organic phase (o) comprise salts of, for example, tetrabutylammonium, tetraphenylarsonium, or bis(triphenyl-phosphoranylidene)ammonium cations with tetraphenylborate, tertrakis(4-chloro-phenyl)borate, or tetrakis[3,5-bis(trifluoromethyl)phenyl]borate anion. [Pg.616]

FIG. 10 Faradaic admittance coefficient Yq for the interface between 0.1 M LiCl in water and 0.02 M tetrabutylammonium tetraphenylborate ( ) or tetrapentylammonium tetrakis[3,5-bis(tri-fluoromethyl)phenyl]borate ( ) in o-nitrophenyl octyl ether as a function of the interfacial potential difference A y. (From Ref 73.)... [Pg.436]

Interface between two immiscible electrolyte solutions — Figure. Cyclic voltammograms of 0.1 M LiCl in water and 0.01 M tetrabutylammonium tetraphenylb orate (—) or tetrapentylammo-nium tetrakis[3)5-bis(trifluoromethyl)-phenyl]borate ( ) in o-NPOE at a sweep rate of 20 mV s-1, interfacial area 0.14 cm2. Reprinted with permission from [vii]. 1998 Elsevier B.V. [Pg.360]

Oxygen Nucleophile. Uchiro et al. have reported hydrolysis of a thioglycoside bond under very mild conditions using the combination of tetrabutylammonium periodate as oxidant, trityl tetrakis(pentafluorophenyl)borate as Lewis acid catalyst, and HMDO in anhydrous acetonitrile at 0 °C (eq 17). The reaction also proceeded well in the absence of HMDO, using aqueous tri-flic or perchloric acid as catalyst in place of the trityl derivative. The intersaccharidic bond of a disaccharide was found to be stable under these conditions, with no anomerization being observed. [Pg.316]

Py pyrrole, MPy 1-methylpyrrole, PPy polypyrrole, PMPy poly(l-methylpyrrole), EDOT 3,4-ethylenedioxytiophene, PEDOT poly(3,4-ethylenedioxytiophene), MT 3-methylthiophene, PMT poly(3-methylthiopliene), NaPSS sodium polystyrene sulfonate, NaDBS sodium dodecylbenzenesulfonate, NaPTS sodium para-toluene sulfonate, BSA benzenesulfonic acid, SSA 2-hydroxy-5-sulfobenzoic acid, MES 2-(Af-morpholino) ethanesulfonic acid, MOPS 3-(Al-morpholino) propanesulfonic acid, PIPES piperazine-l,4-bis(2-ethanesulfonic) acid, MeCN acetonitrile, DCE 1,2-dichloroetane, BU4NPF6 tetrabutylammonium hexafluor-ophosphate, BTPPA-CIO4 bis(triphenylphosphoranylidene)ammonium perchlorate, BTPPA-TFPB bis(triphenylphosphoranylidene)ammonium tetrakis[3,5-bis (trifluoromethyl)phenyl]borate, TPenA tetraphenylammonium... [Pg.323]


See other pages where Tetrabutylammonium tetrakis borate is mentioned: [Pg.740]    [Pg.108]    [Pg.109]    [Pg.111]    [Pg.111]    [Pg.743]    [Pg.108]    [Pg.109]    [Pg.111]    [Pg.494]    [Pg.144]    [Pg.360]    [Pg.401]    [Pg.401]    [Pg.67]    [Pg.360]    [Pg.9]   


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