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Dialkyl- and Diarylboryl Complexes

The base-stabilized BH2 complex Cp Fe(CO)2(BH2-PMe3) (8.72, Fig. 24), has been synthesized via two routes photolytic methane elimination and salt elimination. The upheld 11B NMR chemical shift for this complex (8b -25.1) is indicative of a four-coordinate boron centre [98]. Likewise, the long Fe-B bond measured for the ethyltetramethylcyclopentadienyl derivative ( 75-C5Me4Et)Fe(CO)2(BH2-PMe3) [8.73, 2.195(14) A] and the very low carbonyl stretching frequencies (1932, 1869 cm-1), are as expected for a four-coordinate base-stabilized system [c.f. 2.129(3) A and 1958, 1899 cm-1 for Cp Fe(CO)2(BCl2 4pic), 8.42]. [Pg.69]

Ruthenium boryl complexes containing catecholate, pinacolate and dithi-olate substituents have been analyzed as potential alkane functionalization [Pg.71]

25 Ruthenium boryl systems studied in the functionalization of alkanes (8.91-8.95) [Pg.72]


See other pages where Dialkyl- and Diarylboryl Complexes is mentioned: [Pg.49]    [Pg.68]   


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Dialkyl complexes

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