Chemical Consequences of Unsaturation in Cyclic Organoboranes.
Abstract
The physical and chemical consequences of the potential p(pi)-p(pi) effect in unsaturated, cyclic organoboranes have been studied. The first phase of research was devoted to the synthesis of the requisite cyclic ring systems: three-membered borirene, four-membered cationic borete, five-membered borole, six-membered borabenzene, and seven-membered borepin, fully carbon conjugated rings. The second phase dealt with employing physical methods to assess the extent of carbon-boron conjugation. (Author)
Document Details
- Document Type
- Technical Report
- Publication Date
- Jul 31, 1972
- Accession Number
- AD0748893
Entities
People
- John J. Eisch
Organizations
- The Catholic University of America