在双面玻表面上进行有机合成:具有十二倍功能的密合体结构
Tiejun Li1, Satish S Jalisatgi, Michael J Bayer
1Department of Chemistry and Biochemistry, University of California, Los Angeles, 607 Charles E. Young Drive East, Los Angeles, California 90095, USA.
Journal of the American Chemical Society
|December 15, 2005
概括
通过使用各种方法合成了新型与结合的集群,称为闭合体. 使用1.1'-carbonyldiimidazole激活的碳素酸的一般策略被证明是有效的,用于创建这些多功能集群衍生物.
科学领域:
- 无机化学 无机化学
- 材料科学 材料科学 材料科学
- 集团化学 集团化学
背景情况:
- [closo-B12(OH) [12]2-集群是一种独特的二面体结构,具有潜在的应用.
- 集群的功能化对于调整它们的特性至关重要.
- 乙链接为修改集群表面提供了一条通用途径.
研究的目的:
- 开发和描述新型结衍生物的合成方法[closo-B12(OH) 12) 2-集群 (闭合体).
- 建立一个通用和高效的合成策略来制造这些密闭体.
- 证明开发的方法与各种外围功能组的兼容性.
主要方法:
- 双甲基) - - 克洛索-多德卡基-多德卡酸与活性炭酸,酸化物,无水化物和乙烯基的反应.
- 作为一般的策略,利用1.1'-carbonyldiimidazole (CDI) 进行碳酸激活.
- 使用高温和高压来加速合成.
- 使用固定清除剂试剂,以有效净化闭合体.
主要成果:
- 通过使用多种合成途径成功合成了二二甲的闭合体.
- 确定1.1'-碳基胺醇方法作为一种通用和可靠的合成策略.
- 证明与各种外围功能群的兼容性,包括终端氨基群.
- 制备并随后乙化一个含有十二个末端氨基基组的闭合体.
结论:
- 开发了用于新型结聚衍生物 (闭合) 的多功能合成方法.
- 1,1'-碳乙烯胺醇激活方法是密封体合成的强大和可通用的方法.
- 该方法允许纳入各种功能组,扩大集群的潜在应用.
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