1998
DOI: 10.1021/om980393z
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Group 14 Metalloles with Thienyl Groups on 2,5-Positions:  Effects of Group 14 Elements on Their π-Electronic Structures

Abstract: A series of group 14 metalloles, from silole to stannole, together with cyclopentadiene, having two thienyl groups at the 2,5-positions, have been prepared. Their crystal structures, UV−vis absorption and fluorescence spectra, and cyclic voltammograms have been determined. Theoretical calculations on their electronic structures have also been carried out. On the basis of these experimental and theoretical results, we compared their properties and electronic structures. The group 14 metallole derivatives from s… Show more

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Cited by 142 publications
(143 citation statements)
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“…In principle, a similar stabilizing effect is also expected for the case of the highest occupied molecular orbital (HOMO) in -conjugated systems. [40,41] However, as recently observed by Lu et al, [40] …”
Section: Resultsmentioning
confidence: 79%
“…In principle, a similar stabilizing effect is also expected for the case of the highest occupied molecular orbital (HOMO) in -conjugated systems. [40,41] However, as recently observed by Lu et al, [40] …”
Section: Resultsmentioning
confidence: 79%
“…Recent theoretical studies showed that this bathochromic shift is due to a better interaction between the HOMO of phosphole with the HOMO of thiophene, compared to that of pyridine [6b,8]. It is worth to note that the value of k max recorded for 3a (412 nm) [6a ,b] is considerably more red-shifted than that of the related tert-thiophene (355 nm) [9]. This observation is in agreement with theoretical studies predicting that heterocyclopentadienes with a low aromatic character are optimal building blocks for the synthesis of extended p-conjugated systems with low HOMO-LUMO gap [1h,6d].…”
Section: Physical Propertiesmentioning
confidence: 98%
“…These solid state data suggest a delocalisation of the psystem over the thienyl substituents and the endocyclic p-system of the phosphole ring. The value of k max recorded for (3a) (412 nm) [9a] and (3b) (490 nm) [9c] are considerably more red-shifted than those of related tert-thiophene (355 nm) [10] and quinquethiophenes (ca. 418 nm) [11], respectively.…”
Section: Co-oligomers Containing Phosphole Ringsmentioning
confidence: 99%