| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273272 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
The inductive release of electron density into a dipyrromethene moiety, coordinated to a BF2 group, from a phenyl group variously substituted by ortho- and para-amino groups resulted in relatively strong hydrogen-bonding, whereas the meta-analog formed only weak hydrogen-bonds.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ji-Young Shin, Brian O. Patrick, David Dolphin,