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1,7-Dioxa [7] (2, 7) pyrenophane: The Pyrene Moiety Is More Bent than That of C_(70)

机译:1,7-二恶英[7](2,7)en苯:比C_(70)的B部分更易弯曲

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摘要

The synthesis of the highly strained title compound 8a was achieved by the valence isomerization and in situ dehydrogenation of the cyclophanediene 7a at only 80 deg C. A single-crystal X-ray structure determination of 8a revealed that the pyrene moiety is remarkably bent, the two ends forming an angle of 109.2 deg. This degree of lengthwise bend slightly exceeds that present in the pyrene unit found in the equator of D_(5h) C_(70), rendering it the most bent pyrene group yet prepared. The expectation of unusual reactivity is borne out by the apparent Diels-Alder reaction between 8a and tetracyanoethylene (TCNE) to give adduct 9.
机译:通过仅在80摄氏度下环戊二烯7a的化合价和原位脱氢反应,完成了高张力标题化合物8a的合成。8a的X射线单晶结构测定表明the部分显着弯曲,两端形成109.2度的角度。这种纵向弯曲的程度略大于D_(5h)C_(70)的赤道中发现的the单元中存在的弯曲程度,使其成为迄今制备的最弯曲的pyr基。 8a与四氰基乙烯(TCNE)之间明显的Diels-Alder反应生成加合物9证实了对异常反应活性的预期。

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