<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Casali, Lucia</style></author><author><style face="normal" font="default" size="100%">Mazzei, Luca</style></author><author><style face="normal" font="default" size="100%">Shemchuk, Oleksii</style></author><author><style face="normal" font="default" size="100%">Sharma, Lohit</style></author><author><style face="normal" font="default" size="100%">Honer, Kenneth</style></author><author><style face="normal" font="default" size="100%">Grepioni, Fabrizia</style></author><author><style face="normal" font="default" size="100%">Ciurli, Stefano</style></author><author><style face="normal" font="default" size="100%">Braga, Dario</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Novel Dual-Action Plant Fertilizer and Urease Inhibitor: Urea·Catechol Cocrystal. Characterization and Environmental Reactivity</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Sustainable Chemistry &amp; Engineering</style></secondary-title><short-title><style face="normal" font="default" size="100%">ACS Sustainable Chem. Eng.</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019/01/22</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acssuschemeng.8b06293</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">2852 - 2859</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">2</style></issue><notes><style face="normal" font="default" size="100%">doi: 10.1021/acssuschemeng.8b06293</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hutchins, Kristin M.</style></author><author><style face="normal" font="default" size="100%">Rupasinghe, Thilini P.</style></author><author><style face="normal" font="default" size="100%">Ditzler, Lindsay R.</style></author><author><style face="normal" font="default" size="100%">Swenson, Dale C.</style></author><author><style face="normal" font="default" size="100%">Sander, John R. G.</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Tivanski, Alexei V.</style></author><author><style face="normal" font="default" size="100%">MacGillivray, Leonard R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanocrystals of Metal-Organic Complex Exhibit Remarkably High Conductivity that Increases in Single-Crystal-to-Single-Crystal Transformation.</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Chemical Society</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">nanocrystal Metal Org complex exhibit remarkably high cond increases</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">136</style></volume><pages><style face="normal" font="default" size="100%">6778 - 6781</style></pages><isbn><style face="normal" font="default" size="100%">0002-7863</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">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)]</style></abstract><issue><style face="normal" font="default" size="100%">19</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2014:670885(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Verdugo, Edgard M.</style></author><author><style face="normal" font="default" size="100%">Krause, Caitlin</style></author><author><style face="normal" font="default" size="100%">Genskow, Kelly</style></author><author><style face="normal" font="default" size="100%">Han, Ying</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Mattes, Timothy E.</style></author><author><style face="normal" font="default" size="100%">Valentine, Richard L.</style></author><author><style face="normal" font="default" size="100%">Cwiertny, David M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">N-Functionalized Carbon Nanotubes As a Source and Precursor of N-Nitrosodimethylamine: Implications for Environmental Fate, Transport, and Toxicity.</style></title><secondary-title><style face="normal" font="default" size="100%">Environmental Science &amp; Technology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">nitrogen functionalized carbon nanotube arsenic source precursor nitrosodimethylamine toxicity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">48</style></volume><pages><style face="normal" font="default" size="100%">9279 - 9287</style></pages><isbn><style face="normal" font="default" size="100%">0013-936X</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">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)]</style></abstract><issue><style face="normal" font="default" size="100%">16</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2014:1233176(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Laird, Rebecca C.</style></author><author><style face="normal" font="default" size="100%">Nguyen, Nam P.</style></author><author><style face="normal" font="default" size="100%">Rusch, Sara F.</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">MacGillivray, Leonard R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Noncentrosymmetric Packings Influenced by Electronic Properties of Products of Click Reactions.</style></title><secondary-title><style face="normal" font="default" size="100%">Crystal Growth &amp; Design</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">noncentrosym packing electronic property product click reaction D3LYP PXRD</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">893 - 896</style></pages><isbn><style face="normal" font="default" size="100%">1528-7483</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">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)]</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2014:263112(Journal; Online Computer File)</style></notes></record></records></xml>