Electronic spectra of polymers with conjugated bonds

Drabkin, I. A.; Tsaryuk, V. I.; Cherkashin, Μ. I.; Kisilitsa, P. P.; Chauser, M. G.; Chigir, A. N.; Берлин, А. А.

doi:10.1016/0032-3950(68)90289-x

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Cited by 11 publications

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“…C( 8)-C( 7)-N( 6 C( 10)-C(l 1)-C( 13) 120.4(4) 0( 14)-C(5)-0(4) 122.9(4) C ( 12)-C( 11 )-C( 13) 120.4( 4) C( 7)-N(6)-C( 5) C(8)-C(7)-C (12) 126.0(4) 119.2(4) C( 7)-C( 12)-C(ll) 120.8 (4) 0 C-H lengths range from 0.93 (4) to 1.06 (5) A. 5) and 2.12 (5) A, respectively, and the N-H-O angles is 168 (4)0.25 This hydrogen bonding may be the factor that causes glide-related rather than translationally related diacetylene groups to be in close contact.…”

Section: Discussionmentioning

confidence: 99%

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Solid state phase transformation of a diacetylene by solvation. Crystal structure of a moderately reactive monomer form

Patel¹,

Duesler²,

Curtin³

et al. 1980

J. Am. Chem. Soc.

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Section: Discussionmentioning

confidence: 99%

“…The intensities of three standard reflections indicated an average drop of 10% by the end of the data collection (ca. 4 days); one of the standards (060) dropped by 20%. Of the 2252 independent reflections collected, 1189 were considered nonzero at the 1.5(7 level of significance.…”

Section: Methodsmentioning

confidence: 99%