2003
DOI: 10.1023/b:silc.0000047925.29573.88
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New aryl ethynylene substituted silicon-centered molecules

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Cited by 2 publications
(2 citation statements)
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“…Previously, we were successful in the synthesis of some arylethynyl substituted silicon-centered [22] or related bulky organosilicon compounds showing the property of crystalline inclusion formation [23]. Here, we report on the crystal structures of four tetrakis(arylethynyl)silanes (1)(2)(3)(4) differing in the substitution of the aryl rings, including also compound 5 which is an analogue of 4 without the ethynylene units (Scheme 1).…”
Section: Introductionmentioning
confidence: 95%
“…Previously, we were successful in the synthesis of some arylethynyl substituted silicon-centered [22] or related bulky organosilicon compounds showing the property of crystalline inclusion formation [23]. Here, we report on the crystal structures of four tetrakis(arylethynyl)silanes (1)(2)(3)(4) differing in the substitution of the aryl rings, including also compound 5 which is an analogue of 4 without the ethynylene units (Scheme 1).…”
Section: Introductionmentioning
confidence: 95%
“…The Si–CCpeak has a chemical shift of 108–109 ppm, while a CC iso to an aromatic carbon peak has a chemical shift of 88–89 ppm. These peaks are characteristic of aromatic ethynylsilanes. …”
Section: Resultsmentioning
confidence: 99%