<?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%">Taifan, William</style></author><author><style face="normal" font="default" size="100%">E.</style></author><author><style face="normal" font="default" size="100%">Li, Yuanyuan</style></author><author><style face="normal" font="default" size="100%">Baltrus, John P.</style></author><author><style face="normal" font="default" size="100%">Zhang, Lihua</style></author><author><style face="normal" font="default" size="100%">Frenkel, Anatoly I.</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%">Operando Structure Determination of Cu and Zn on Supported MgO/SiO2 Catalysts during Ethanol Conversion to 1,3-Butadiene</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Catalysis</style></secondary-title><short-title><style face="normal" font="default" size="100%">ACS Catal.</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%">2019/01/04</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acscatal.8b03515</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%">9</style></volume><pages><style face="normal" font="default" size="100%">269 - 285</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">doi: 10.1021/acscatal.8b03515</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%">Kiani, Daniyal</style></author><author><style face="normal" font="default" size="100%">Sourav, Sagar</style></author><author><style face="normal" font="default" size="100%">Wachs, Israel E.</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%">The Oxidative Coupling of Methane (OCM) by SiO2-Supported Tungsten Oxide Catalysts Promoted with Mn and Na</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Catalysis</style></secondary-title><short-title><style face="normal" font="default" size="100%">ACS Catal.</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%">2019/05/22</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://pubs.acs.org/doi/abs/10.1021/acscatal.9b01585</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%">9</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">7</style></issue><notes><style face="normal" font="default" size="100%">doi: 10.1021/acscatal.9b01585</style></notes><section><style face="normal" font="default" size="100%">5912-5928</style></section></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%">Elacqua, Elizabeth</style></author><author><style face="normal" font="default" size="100%">Jurgens, Paul T.</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%">Organic nanocrystals of [2.2]paracyclophanes achieved via sonochemistry: enhanced and red-shifted emission involving edge-to-face chromophores.</style></title><secondary-title><style face="normal" font="default" size="100%">CrystEngComm</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">org nanocrystal paracyclophane via sonochem</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2012///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">7567 - 7571</style></pages><isbn><style face="normal" font="default" size="100%">1466-8033</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">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)]</style></abstract><issue><style face="normal" font="default" size="100%">22</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2012:1517546(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%">Sander, John R. G.</style></author><author><style face="normal" font="default" size="100%">Bucar, Dejan-Kresimir</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%">Organic Nanocrystals of the Resorcinarene Hexamer via Sonochemistry: Evidence of Reversed Crystal Growth Involving Hollow Morphologies.</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%">morphol resorcinarene hexamer nanocrystal sonochem reversed crystal growth</style></keyword><keyword><style  face="normal" font="default" size="100%">org nanocrystal resorcinarene hexamer sonochem reversed crystal growth</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2012///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">134</style></volume><pages><style face="normal" font="default" size="100%">6900 - 6903</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%">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)]</style></abstract><issue><style face="normal" font="default" size="100%">16</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2012:219467(Journal; Online Computer File)</style></notes></record></records></xml>