...
首页> 外文期刊>Angewandte Chemie >Access to Extended Polyphosphorus Frameworks
【24h】

Access to Extended Polyphosphorus Frameworks

机译:访问扩展的多磷框架

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The activation of P4 is an current topic in chemistry. Recently, a big impact was made by main-group elements that are able to open one, two,or three P—P bonds and can degrade the P4 moiety to a P2 or P1 unit. Aggregation of P4 by N-heterocyclic carbenes (NHCs) has also shown that the large P_(12) unit in A can be achieved. Moreover, larger cationic P_n~+ (n ≤ 89) and anionic P_n~- (n ≤ 49) polyphosphorus species have been generated in the gas phase using laser ablation techniques. Earlier investigations in organic solvents by Baudler and co-workers led to a large number of organo-substituted polyphosphorus compounds. They have also achieved the synthesis of mixtures of the larger polyphos-phides, such as P_(16)~(2-), P_(19)~(3-), and P_(21) Some of these structures were partially isolated and structurally characterized as was the polyphosphide P_(26)~(4-).
机译:P4的激活是化学领域的当前话题。最近,能够打开一个,两个或三个P-P键并将P4部分降解为P2或P1单元的主族元素产生了巨大影响。 N杂环卡宾(NHC)对P4的聚集也表明,可以实现A中较大的P_(12)单元。此外,使用激光烧蚀技术在气相中产生了较大的阳离子P_n〜+(n≤89)和阴离子P_n〜-(n≤49)多磷物质。鲍德勒及其同事对有机溶剂的早期研究导致了大量有机取代的多磷化合物。他们还实现了较大的多磷酸盐混合物的合成,例如P_(16)〜(2-),P_(19)〜(3-)和P_(21)。在结构上表征为多磷化物P_(26)〜(4-)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号