Synthesis, characterization, and crystal structures of two strained cyclic diacetylenes and their precursors |
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Authors: | Kyle P Baldwin Richard S Simons Daniel A Scheiman Robert Lattimer Claire A Tessier Wiley J Youngs |
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Institution: | (1) Department of Chemistry, University of Akron, Akron, Ohio, 44325-3601;(2) Nyma INC., 21000 Brookpark Road, Cleveland, Ohio, 44135;(3) BFGoodrich, Brecksville Road, Brecksville, Ohio, 44141 |
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Abstract: | The synthesis, characterization, and crystal structures of two novel strained cyclic diacetylenes are reported. A discussion is presented about the relative bond distances of the diacetylenes compared to a previously reported strained cyclic diacetylene to further determine the degree of aromaticity of that compound. 1,2:5,6:9,10:13,14-Tetrabenzo-3,7,11,15,17-pentadehydro18] annulene (5) is triclinic, P
–1, with = 9.489(5), b = 10.550(5), c = 12.155(6) Å, = 100.50(4), = 106.50(4), = 100.85(4)°. 1,2:5,6:9,10:13,14:17,18-Pentabenzo-3,7,11,15,19,23,25-heptadehydro26]annulene (7) is triclinic, P
–1, with a = 9.611(2), b = 10.388(3), c = 15.963(3) Å, = 88.67(2), = 76.25(1), = 68.69(2). In addition, two precursors of 5, 3 and 4 which have a helical twist, are reported. 1,2-ethynediyl-bis(2,1-phenylene-2,1-ethynediyl-2,1-phenylene-2,1-ethynediyl]bistrimethyl-silane] (3) is monoclinic, P21/c, with a = 13.682(4), b = 9.787(2), c = 13.448(4) Å, = 112.37(2)°. 1,1 -(1,2-ethynyldiyl)bis2-(2-ethynylphenyl)ethynyl]-benzene (4) is monoclinic, P21/n, with a = 15.951(3), b = 3.999(1), c = 18.168(4) Å, = 99.05(3)°. |
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Keywords: | Cyclyne strained cyclic diyne diacetylene benzo dehydro annulene |
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