@article {350,
	title = {Novel Dual-Action Plant Fertilizer and Urease Inhibitor: Urea{\textperiodcentered}Catechol Cocrystal. Characterization and Environmental Reactivity},
	journal = {ACS Sustainable Chemistry \& Engineering},
	volume = {7},
	year = {2019},
	note = {doi: 10.1021/acssuschemeng.8b06293},
	month = {2019/01/22},
	pages = {2852 - 2859},
	publisher = {American Chemical Society},
	url = {https://doi.org/10.1021/acssuschemeng.8b06293},
	author = {Casali, Lucia and Mazzei, Luca and Shemchuk, Oleksii and Sharma, Lohit and Honer, Kenneth and Grepioni, Fabrizia and Ciurli, Stefano and Braga, Dario and Baltrusaitis, Jonas}
}
@article {89,
	title = {Nanocrystals of Metal-Organic Complex Exhibit Remarkably High Conductivity that Increases in Single-Crystal-to-Single-Crystal Transformation.},
	journal = {Journal of the American Chemical Society},
	volume = {136},
	year = {2014},
	note = {CAPLUS AN 2014:670885(Journal; Online Computer File)},
	pages = {6778 - 6781},
	publisher = {American Chemical Society},
	abstract = {Ag(I) is used to form a π-stacked metal-org. solid that exhibits remarkably high elec. cond.  The solid undergoes a single-crystal-to-single-crystal [2+2] photodimerization to generate a 1D coordination polymer with over 40\% higher cond.  The Ag(I) complex represents the first example of an increase in cond. resulting from a [2+2] photodimerization.  D. of states calcns. show a higher contribution from Ag(I) ions to the valence band in the photodimerized solid, supporting the increase in cond. [on SciFinder(R)]},
	keywords = {nanocrystal Metal Org complex exhibit remarkably high cond increases},
	isbn = {0002-7863},
	author = {Hutchins, Kristin M. and Rupasinghe, Thilini P. and Ditzler, Lindsay R. and Swenson, Dale C. and Sander, John R. G. and Baltrusaitis, Jonas and Tivanski, Alexei V. and MacGillivray, Leonard R.}
}
@article {88,
	title = {N-Functionalized Carbon Nanotubes As a Source and Precursor of N-Nitrosodimethylamine: Implications for Environmental Fate, Transport, and Toxicity.},
	journal = {Environmental Science \& Technology},
	volume = {48},
	year = {2014},
	note = {CAPLUS AN 2014:1233176(Journal; Online Computer File)},
	pages = {9279 - 9287},
	publisher = {American Chemical Society},
	abstract = {Hazardous byproducts may be generated during the environmental processing of engineered nanomaterials.  Here, we explore the ability of carbon nanotubes with nitrogen-contg. surface groups (N-CNTs) to generate N-nitrosodimethylamine (NDMA) during chem. disinfection.  Unexpectedly, we obsd. that com. N-CNTs with amine, amide, or N-contg. polymer (PABS) surface groups are a source of NDMA.  As-received powders can leach up to 50 ng of NDMA per mg of N-CNT in aq. suspension; presumably NDMA originates as a residue from N-CNT manufg.  Furthermore, reaction of N-CNTs with free chlorine, monochloramine, and ozone generated byproduct NDMA at yields comparable to those reported for natural org. matter.  Chlorination also altered N-CNT surface chem., with XPS indicating addn. of Cl, loss of N, and an increase in surface O.  Although these changes can increase N-CNT suspension stability, they do not enhance their acute toxicity in E. coli bioassays above that obsd. for as-received powders.  Notably, however, dechlorination of reacted N-CNTs with sulfite completely suppresses N-CNT toxicity.  Collectively, our work demonstrates that N-CNTs are both a source and precursor of NDMA, a probable human carcinogen, while chem. disinfection can produce CNTs exhibiting surface chem. and environmental behavior distinct from that of native (i.e., as-received) materials. [on SciFinder(R)]},
	keywords = {nitrogen functionalized carbon nanotube arsenic source precursor nitrosodimethylamine toxicity},
	isbn = {0013-936X},
	author = {Verdugo, Edgard M. and Krause, Caitlin and Genskow, Kelly and Han, Ying and Baltrusaitis, Jonas and Mattes, Timothy E. and Valentine, Richard L. and Cwiertny, David M.}
}
@article {90,
	title = {Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions.},
	journal = {Crystal Growth \& Design},
	volume = {14},
	year = {2014},
	note = {CAPLUS AN 2014:263112(Journal; Online Computer File)},
	pages = {893 - 896},
	publisher = {American Chemical Society},
	abstract = {Though 1,4-disubstituted 1,2,3-triazole rings have been utilized as electronic bridges in the soln. phase, the use of a triazole ring to serve as an electronic bridge of small mols. in the cryst. state has been underdeveloped.  Here two compds. with a central 1,4-disubstituted 1,2,3-triazole ring are synthesized to investigate the electronic bridging between terminal stilbazole and pyridine groups in the cryst. phase.  The electronic properties of the mols. are characterized through soln. phase UV-vis spectroscopy, single crystal X-ray diffractions, and d.-of-state and gas-phase DFT calcns.  We show that the electronic bridging behavior of a 1,4-disubstituted 1,2,3-triazole ring derived from a click reaction is maintained in the solid state by rare head-to-head (hh) packing in noncentrosym. crystal environments. [on SciFinder(R)]},
	keywords = {noncentrosym packing electronic property product click reaction D3LYP PXRD},
	isbn = {1528-7483},
	author = {Laird, Rebecca C. and Nguyen, Nam P. and Rusch, Sara F. and Baltrusaitis, Jonas and MacGillivray, Leonard R.}
}
