1975
DOI: 10.1007/bf00747197
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Molecular and crystal structure of 9,9,10,10-tetramethyl-9,10-disiladihydroanthracene

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Cited by 3 publications
(6 citation statements)
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“…The Si−C−C bond angles of the disilacyclohexadiene rings (average 124.1°) are larger than those of trans - 3 (average 122.8°), 4 (average 122°),2e and 5 (average 123°) 2c2c. These structural features of cis - 3 seem to be favorable for reducing the steric repulsion among the tert -butyl groups…”
Section: Resultsmentioning
confidence: 90%
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“…The Si−C−C bond angles of the disilacyclohexadiene rings (average 124.1°) are larger than those of trans - 3 (average 122.8°), 4 (average 122°),2e and 5 (average 123°) 2c2c. These structural features of cis - 3 seem to be favorable for reducing the steric repulsion among the tert -butyl groups…”
Section: Resultsmentioning
confidence: 90%
“…The tert -butyl groups occupy less crowded flagpole positions. The Si−C(phenyl) bond lengths (average 1.870 Å) are longer than those of trans - 3 (average 1.861 Å), 4 (average 1.85 Å),2e and 5 (average 1.86 Å) 2c2e and 5 (average 123°) 2c…”
Section: Resultsmentioning
confidence: 94%
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“…However, the observed In−C(phenylene) bonds (2.160(8) and 2.161(8) Å), and especially the In−C(aryl) bonds (2.191(8) Å), are longer than those in (C 6 H 5 ) 3 In (2.111(14)−2.155(14) Å) B, Si, Ge, As, Te 16 ) are planar or have a boat conformation; to our knowledge, there is only one other example of a sterically hindered 9,10-dihydro-9,10-dimetallaanthracene with a chairlike puckering of the central six-membered ring (M = Si) …”
mentioning
confidence: 80%