@article {138,
	title = {Organic nanocrystals of [2.2]paracyclophanes achieved via sonochemistry: enhanced and red-shifted emission involving edge-to-face chromophores.},
	journal = {CrystEngComm},
	volume = {14},
	year = {2012},
	note = {CAPLUS AN 2012:1517546(Journal; Online Computer File)},
	month = {2012///},
	pages = {7567 - 7571},
	publisher = {Royal Society of Chemistry},
	abstract = {We have prepd. org. nanocrystals of [2.2]paracyclophane (pCp) and tetrakis(4-pyridylcyclobutyl)[2.2]paracyclophane (tpcp) via sonochem.  Both nanocrystals exhibit an enhanced fluorescence compared to dil. soln., while the tpcp nanocrystals also demonstrate a red-shifted fluorescence. [on SciFinder(R)]},
	keywords = {org nanocrystal paracyclophane via sonochem},
	isbn = {1466-8033},
	author = {Elacqua, Elizabeth and Jurgens, Paul T. and Baltrusaitis, Jonas and MacGillivray, Leonard R.}
}
@article {174,
	title = {Dramatic Red-Shifted Fluorescence of [2.2]Paracyclophanes with Peripheral Substituents Attached to the Saturated Bridges.},
	journal = {Organic Letters},
	volume = {11},
	year = {2009},
	note = {CAPLUS AN 2009:1306162(Journal)},
	month = {2009///},
	pages = {5106 - 5109},
	publisher = {American Chemical Society},
	abstract = {A bridge-substituted [2.2]paracyclophane (I) obtained from the org. solid state exhibits a dramatic red shift in fluorescence relative to [2.2]paracyclophane.  A further red shift occurs upon alkylation of the pyridylcyclobutyl bridges (II; R = Me, Et).  Our results demonstrate that [2.2]cyclophanes substituted at the bridge, despite not being attached via the extended π-system, are promising building blocks in the development of optical materials. [on SciFinder(R)]},
	keywords = {red shifted fluorescence paracyclophane pyridinium salt prepn},
	isbn = {1523-7060},
	author = {Elacqua, Elizabeth and Bucar, Dejan-Kresimir and Skvortsova, Yulia and Baltrusaitis, Jonas and Geng, M. Lei and MacGillivray, Leonard R.}
}
