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Bis -cyclopentadienyl 1,2-dimethoxyethane ytterbium II

Work-up, as above, gives the pure complex as green crystals. Yield 1.40 g (96%). (The checkers isolation method gave 68%). [Pg.296]

Shriver, TTte Manipulation of Air-Sensitive Compounds, McGraw-Hill, New York, 1969. [Pg.297]

Transition-Metal Compounds, in Organometallic Syntheses, Vol. I, J. J. Eisch and R. B. King (eds.), 1965 Vol. 2, J. J. Eisch, Nontransition-Metal Compounds, 1981 Academic Press, New York. [Pg.297]

Submitted by WILLIAM J. EVANS and TAMARA A. UUBARRI Checked by HERBERT SCHUMANN and SIEGBERT NICKEL [Pg.297]

The complexes described below are extremely air and moisture sensitive. Therefore, the syntheses are conducted under nitrogen with rigorous exclusion of air and water by using Schlenk, vacuum-line, and glove-box techniques.  [Pg.298]




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1 2 Dimethoxyethane

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Ytterbium bis

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