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Synthesis and X-ray Crystallographic Characterization of Spiro Orthocarbonates
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  • Synthesis and X-ray Crystallographic Characterization of Spiro Orthocarbonates
  • Synthesis and X-ray Crystallographic Characterization of Spiro Orthocarbonates
저자명
Park. Young Ja,No. Kwang Hyun,Kim. Ju Hee,Suh. Il-Hwan
간행물명
Bulletin of the Korean Chemical Society
권/호정보
1992년|13권 4호|pp.375-381 (7 pages)
발행정보
대한화학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

In this study we have synthesized two spiro orthocarbonates, which can be polymerized with volume expansion, and determined their crystal structures. The crystal data are as follows; 3,4,10,11-Di(9,10-dihydro-9,10-ethanoanthracenyl)- 1,6,8,13-tetraoxa-6.6-tridecane 5: a = 16.898 (1), b = 9.299 (1), c = 24.359 (2) ${AA}$, $eta$ = 123.73 $(7)^{circ}$, space group P21/c and R = 0.073 for 2954 reflections; compound 8: a = 15.244 (4), b = 15.293 (3), c = 10.772 (3) $AA$, ${eta}$ = 99.45 $(2)^{circ}$, space group P21/c and R = 0.082 for 2346 reflections. The seven-membered rings of compound 5 are chair forms and all the six-membered rings are boat shaped. For a six-membered spiro orthocarbonate, 3,9-Di(9-fluorenylidenyl)-1,4,6,9-tetraoxa-5,5-und ecane 8, fluorene groups [C(1) atom through C(13) atom] are planar within ${pm}0.09{AA}$ and the six-membered rings have chair conformations. The whole molecule has pseudo-C2 symmetry. The water molecules in the crystal are linked with each other through the hydrogen bond with distance of 2.790 (20) ${AA}$.