@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 {139,
	title = {Organic Nanocrystals of the Resorcinarene Hexamer via Sonochemistry: Evidence of Reversed Crystal Growth Involving Hollow Morphologies.},
	journal = {Journal of the American Chemical Society},
	volume = {134},
	year = {2012},
	note = {CAPLUS AN 2012:219467(Journal; Online Computer File)},
	month = {2012///},
	pages = {6900 - 6903},
	publisher = {American Chemical Society},
	abstract = {Nano- and micrometer-scale crystals of a self-assembled hexamer were synthesized via sonochem.  The application of ultrasonic irradn. afforded hollow rhombic-dodecahedral crystals of the C-methylcalix[4]resorcinarene hexamer.  The formation of the hollow crystals is attributed to a reversed crystal growth mechanism heretofore described only in the synthesis of inorg.-based materials. [on SciFinder(R)]},
	keywords = {morphol resorcinarene hexamer nanocrystal sonochem reversed crystal growth, org nanocrystal resorcinarene hexamer sonochem reversed crystal growth},
	isbn = {0002-7863},
	author = {Sander, John R. G. and Bucar, Dejan-Kresimir and Baltrusaitis, Jonas and MacGillivray, Leonard R.}
}
