@article {2249,
	title = {Self-assembly via intermolecular hydrogen-bonding between o-/m-/p-NH2 and BF2 groups on dipyrromethenes},
	journal = {Tetrahedron Letters},
	volume = {49},
	number = {38},
	year = {2008},
	note = {ISI Document Delivery No.: 349UTTimes Cited: 0Cited Reference Count: 17Shin, Ji-Young Patrick, Brian O. Dolphin, David},
	month = {Sep},
	pages = {5515-5518},
	type = {Article},
	abstract = {Boron difluoride dipyrromethenes bearing configurationally different amine groups on a meso-phenyl ring were prepared and crystallized. The ortho- and para-amino groups allow the phenyl group to inductively release greater electron density into the dipyrromethenes resulting in relatively strong intermolecular hydrogen-bonding with the terminal BF2 groups, whereas the meta-analog formed weaker hydrogen-bonds. The intensities of the H-1 NMR peaks in concentrated solutions all increased with F-decoupling. (C) 2008 Elsevier Ltd. All rights reserved.},
	keywords = {ANALOG, boron-dipyrromethene, CHEMISTRY, EFFICIENT, HYDROGEN-BOND, LIGANDS, MOLECULES, self-assembly, SOLID-STATE},
	isbn = {0040-4039},
	url = {<Go to ISI>://000259309500020},
	author = {Shin, J. Y. and Patrick, B. O. and Dolphin, D.}
}
