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Stibine, triethyl

Stibine, (o-bromophenyl)dichloro-, 1007 Stibine, chlorodimethyl-, 1007 Stibine, chlorodiphenyl-, 1007 Stibine, ethylenebis(diphenyl-, 1008 Stibine, ethylidynebis(dimethyl-, 1008 Stibine, o-phenylenebis(dimethyl-, 1008 Stibine, triethyl-, 1008 Stibine, trimethyl-, 1008 Stibine, triphenyl-, 1008 sulfide... [Pg.1743]

Antimony Pentasulfide. See under Sulfides Antimony Selenide. See under Selenides Antimony Sulfides. See under Sulfides Antimony Telluride, See under Tellurides Antimony Trichloride. See under Chlorides Antimony Triethyl. Same as Triethylstibine Antimony Trimethyl. Same as Trimethyl-stibine... [Pg.470]

There are direct measurements of the dissociation enthalpy for cleaving the first bond in trimethylarsine, -stibine and -bismuthine, and triethyl-stibine and convincing evidence that these R—ER2 bounds have significantly different dissociation enthalpies from the subsequent RE—R and R—E bonds. Reliable measurement of the enthalpy of formation of the various McjE species and the E—E bond enthalpies in the... [Pg.165]

Polyphosphines can be made by reduction of a phosphonous dihalide with a metal such as Li, Na, Mg or Hg, or with lithium aluminium hydride (6.680). They are also obtained on heating a phosphonous dihalide with tributyl phosphine (6.681), or triethyl stibine (6.682), or simply heating a phosphonous difluoride in a sealed tube (6.515). [Pg.423]


See other pages where Stibine, triethyl is mentioned: [Pg.225]    [Pg.1097]    [Pg.225]    [Pg.1097]    [Pg.813]    [Pg.448]    [Pg.158]    [Pg.299]    [Pg.175]    [Pg.182]    [Pg.175]    [Pg.182]    [Pg.546]    [Pg.174]   
See also in sourсe #XX -- [ Pg.2 , Pg.1008 ]




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