{"id":32,"date":"2018-01-01T02:05:20","date_gmt":"2018-01-01T02:05:20","guid":{"rendered":"http:\/\/commons.ggc.edu\/amallia\/?page_id=32"},"modified":"2023-04-05T23:34:24","modified_gmt":"2023-04-05T23:34:24","slug":"publications","status":"publish","type":"page","link":"https:\/\/commons.ggc.edu\/amallia\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"<p><em>Undergraduate co-authors are underlined and high school students are italicized. <\/em><\/p>\n<p>46. Mallia, A.; Sloop, J. Advances in the Synthesis of Heteroaromatic Hybrid Chalcones. <a href=\"https:\/\/www.mdpi.com\/1420-3049\/28\/7\/3201\" target=\"_blank\" rel=\"noopener\"><em>Molecules<\/em> <\/a>2023, 28(7), 3201; https:\/\/doi.org\/10.3390\/molecules28073201<\/p>\n<p>45.<u> Faass, M.<\/u>; <strong>Mallia, A.<\/strong>; Sommer, R., Sloop, J. (Z)-2-(3, 5-Dimethoxybenzylidene) Indan-1-one. CCDC 2081969: Experimental Crystal Structure Determination. <a href=\"https:\/\/www.ccdc.cam.ac.uk\/structures\/Search?Author=Joseph%20Sloop&amp;JTitle=CSD%20Communication&amp;Year=2021&amp;DatabaseToSearch=Published\" target=\"_blank\" rel=\"noopener\"><em>CSD Communication<\/em><\/a>, <strong>2021, <\/strong>DOI: 10.5517\/ccdc.csd.cc27wg9x.<\/p>\n<p>44. Boyle, P., Breaud, D.; Churley, M.; Coppock, P.; <u>Encarnacion-Thomas, E<\/u>.;, <u>Fernandes, C<\/u>.; Fountain, A.; Gomez, C.; Guzman, A.; Jackson, J.; Lam, L.; <strong>Mallia, A<\/strong>.; Moseley, S.; Park, S.; Pearman, W.; Schmidt, R.; Sloop, J.; Sommer, R.; Stalker, S.; Weyand, J; <u>Wilmott, K<\/u>.;, Yi, J. \u201cSynthesis and Structural Features of Indanone, Tetralone and Naphthone Derivatives: Selective Fluorination and Condensation Products,\u201d Chapter 2 in <a href=\"https:\/\/bp.bookpi.org\/index.php\/bpi\/catalog\/book\/302\" target=\"_blank\" rel=\"noopener\">Current Perspectives on Chemical Sciences<\/a>, Volume 2, edited by H. Sutar, Book Publisher International, London, UK, 2020, 16 pages. ISBN: 978-93-90431-43-4 (Print), 978-93-90431-51-9 (e-Book). DOI: https:\/\/doi.org\/10.9734\/bpi\/cpcs\/v2.<\/p>\n<p>43. Anzovino, M. E.; <strong>Mallia, V. A.<\/strong>; Morton, M. S.; \u00a0Barker, \u00a0Paredes, J. E. B.; Pennington, R.; \u00a0David P. Pursell, D. P.; Rudd, G. E. A.; \u00a0Shepler, B. ; Villanueva, O.; Lee, S. Insights and Initiatives While Teaching Organic Chemistry I and II with Laboratory Courses in the Time of COVID-19. <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jchemed.0c00766\" target=\"_blank\" rel=\"noopener\"><em>J. Chem. Educ.<\/em><\/a> 2020, 000.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-809 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ed0c00766_0001-300x120.jpeg\" alt=\"\" width=\"565\" height=\"226\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ed0c00766_0001-300x120.jpeg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ed0c00766_0001-768x308.jpeg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ed0c00766_0001-1024x411.jpeg 1024w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ed0c00766_0001-1200x481.jpeg 1200w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ed0c00766_0001-100x40.jpeg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ed0c00766_0001.jpeg 1399w\" sizes=\"auto, (max-width: 565px) 85vw, 565px\" \/><\/p>\n<p>42.\u00a0<strong>Mallia,\u00a0V. A<\/strong>. Self-assembly and aggregation studies of simple structural derivatives of stearic acid. <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/bk-2020-1355.ch003\" target=\"_blank\" rel=\"noopener\"><em>ACS Symp. Ser.<\/em><\/a><strong> 2020<\/strong>, <em>000<\/em>.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-806 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/coi-300x106.jpg\" alt=\"\" width=\"486\" height=\"172\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/coi-300x106.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/coi-768x270.jpg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/coi-1024x361.jpg 1024w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/coi-100x35.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/coi.jpg 1031w\" sizes=\"auto, (max-width: 486px) 85vw, 486px\" \/><\/p>\n<p>41.\u00a0Encarnacion-Thomas, E.; Sommer, R. D.; <strong>Mallia, V. A.<\/strong>; Sloop, J. (E)-2-(3,5-Dimethoxy-benzylidene)indan-1-one. <a href=\"https:\/\/iucrdata.iucr.org\/x\/issues\/2020\/06\/00\/bt4094\/\" target=\"_blank\" rel=\"noopener\"><em>IUCrData <\/em><\/a><strong>2020<\/strong>, <em>5<\/em>, x200759.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-797 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/07\/fig-IUCR-300x167.jpg\" alt=\"\" width=\"300\" height=\"167\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/07\/fig-IUCR-300x167.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/07\/fig-IUCR-768x428.jpg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/07\/fig-IUCR-100x56.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/07\/fig-IUCR.jpg 888w\" sizes=\"auto, (max-width: 300px) 85vw, 300px\" \/><\/p>\n<p>40.<strong> Mallia<\/strong>,<strong> V. A.<\/strong>; Weiss, R. G. Structure-property comparison and self-assembly studies of molecular gels derived from (R)-12-hydroxystearic acid derivatives as low molecular mass gelators. <em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/bk-2018-1296.ch012\">ACS Symp. Ser.<\/a><\/em> 2018, 1296, 227\u2013243.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-348 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/08\/bk-2018-000028_g001.gif\" alt=\"\" width=\"277\" height=\"108\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/08\/bk-2018-000028_g001.gif 120w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/08\/bk-2018-000028_g001-100x39.gif 100w\" sizes=\"auto, (max-width: 277px) 85vw, 277px\" \/><\/p>\n<p>39. Alvarez-Mitre F. M.; <strong>Mallia, V. A.<\/strong>; Weiss, R. G.; Toro-Vazquez, J. F. Self-assembly in vegetable oils of ionic gelators derived from (R)-12-hydroxystearic acid. <em><a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S2213329116300156\">Food Structure<\/a> <\/em><strong>2017, <\/strong>13, 56-69<em>.<\/em><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-35 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2017-foodstructure.jpg\" alt=\"\" width=\"307\" height=\"231\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2017-foodstructure.jpg 266w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2017-foodstructure-100x75.jpg 100w\" sizes=\"auto, (max-width: 307px) 85vw, 307px\" \/><\/p>\n<p>38.<strong> Mallia, V. A.<\/strong>; Samai, S.; Weiss, R. G.; Cholesterol and dihydrocholesterol are simple steroidal molecular gelators: How one double bond controls the structure and mechanotropic properties of their gels. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/slct.201601012\/full\"><em>ChemistrySelect <\/em><\/a><strong>2016, <\/strong><em>1<\/em>, 4965-4972.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-37 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2017-chemistry-select-300x269.jpg\" alt=\"\" width=\"312\" height=\"280\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2017-chemistry-select-300x269.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2017-chemistry-select-301x270.jpg 301w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2017-chemistry-select-100x90.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2017-chemistry-select.jpg 529w\" sizes=\"auto, (max-width: 312px) 85vw, 312px\" \/><\/p>\n<p>37.<strong> Mallia,\u00a0V. A<\/strong>.; Weiss, R. G. Correlations between thixotropic and structural propertis of molecular gels with crystalline networks. <a href=\"http:\/\/pubs.rsc.org\/-\/content\/articlelanding\/2016\/sm\/c6sm00377j\/unauth#!divAbstract\"><em>Soft Matter<\/em> <\/a><strong>2016, <\/strong>12<strong>, <\/strong>3665-3676.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-39 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2016-review-300x187.jpg\" alt=\"\" width=\"319\" height=\"199\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2016-review-300x187.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2016-review-768x478.jpg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2016-review-434x270.jpg 434w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2016-review-100x62.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2016-review.jpg 812w\" sizes=\"auto, (max-width: 319px) 85vw, 319px\" \/><\/p>\n<p>36. <strong>Mallia,\u00a0V. A<\/strong>.; Blair, D. L; Weiss, R. G. Oscillatory rheology and surface water wave effects on crude oil and corn oil gels with <em>(R)-<\/em>12-hydroxystearic acid as gelator. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.iecr.5b04267\"><em>Ind. Eng. Chem. Res. <\/em><\/a><strong>2016<\/strong>, 55, 954-960.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-41 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2016-industrial-eng-300x144.jpg\" alt=\"\" width=\"317\" height=\"152\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2016-industrial-eng-300x144.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2016-industrial-eng-561x270.jpg 561w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2016-industrial-eng-100x48.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2016-industrial-eng.jpg 761w\" sizes=\"auto, (max-width: 317px) 85vw, 317px\" \/><\/p>\n<p>35.<strong> Mallia,\u00a0V. A<\/strong>.; Weiss, R. G. Molecular gels of (<em>R<\/em>)-12-hydroxy-<em>N<\/em>-(\u03c9-hydroxyalkyl)octadecanamides. Structural bases for rates of formation and very fast response to destructive strain. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/sm\/2015\/c5sm00353a#!divAbstract\"><em>Soft Matter<\/em> <\/a><strong>2015<\/strong>, <em>11<\/em>, 5010-5022.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-43 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2015-300x234.jpg\" alt=\"\" width=\"322\" height=\"251\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2015-300x234.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2015-768x598.jpg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2015-347x270.jpg 347w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2015-100x78.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/softmatter-2015.jpg 779w\" sizes=\"auto, (max-width: 322px) 85vw, 322px\" \/><\/p>\n<p>34. M. Rogers, X. Liu, <strong>Mallia,\u00a0V. A<\/strong>.; Weiss, R. G. Dissecting kinetic pathways to formation of the fibrillar objects in molecular gels using synchrotron FT-IR. <a href=\"http:\/\/pubs.rsc.org\/-\/content\/articlelanding\/2015\/ce\/c5ce00733j\/unauth#!divAbstract\"><em>Cryst. Eng. Commun, <\/em><\/a><strong>2015<\/strong><em>, 17, <\/em>8085-8092.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-45 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/crystal-eng-2016-300x211.jpg\" alt=\"\" width=\"376\" height=\"265\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/crystal-eng-2016-300x211.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/crystal-eng-2016-384x270.jpg 384w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/crystal-eng-2016-100x70.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/crystal-eng-2016.jpg 625w\" sizes=\"auto, (max-width: 376px) 85vw, 376px\" \/><\/p>\n<p>33.<strong> Mallia,\u00a0V. A<\/strong>.; Weiss, R. G. Self-assembled fibrillar networks and molecular gels employing 12-hydroxystearic acid and its isomers and derivatives. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/poc.3193\/full\"><em>J. Phys. Org. Chem<\/em>.<\/a> <strong>2014<\/strong>, <em>27<\/em>, 310-315.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-47 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2014-JPOC-review-300x213.jpg\" alt=\"\" width=\"342\" height=\"243\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2014-JPOC-review-300x213.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2014-JPOC-review-380x270.jpg 380w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2014-JPOC-review-100x71.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/2014-JPOC-review.jpg 703w\" sizes=\"auto, (max-width: 342px) 85vw, 342px\" \/><\/p>\n<p>32.<strong> Mallia,\u00a0V. A<\/strong>.; Seo, H.; Weiss, R. G. Influence of anions and alkyl chain lengths of N-alkyl-n-(R)-12-hydroxy octadecyl ammonium salts on their hydrogels and organogels. \u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/la400748q\"><em>Langmuir<\/em><\/a>,\u00a0<strong>2013<\/strong>, <em>29<\/em>, 6476-6484.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-49 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00748q_0007-300x162.jpeg\" alt=\"\" width=\"341\" height=\"184\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00748q_0007-300x162.jpeg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00748q_0007-768x416.jpeg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00748q_0007-499x270.jpeg 499w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00748q_0007-100x54.jpeg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00748q_0007.jpeg 998w\" sizes=\"auto, (max-width: 341px) 85vw, 341px\" \/><\/p>\n<p>31. Bag, B. G.; Majumdar, R.; Dinda, S. K.; Dey, P. P.; Maity, G. C.; <strong>Mallia, V. A.<\/strong>; Weiss, R. G. Self-assembly of ketals of arjunolic acid into vesicles and fibers yielding gel-like dispersions. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/la304485e\"><em>Langmuir<\/em> <\/a><strong>2013<\/strong>, <em>29<\/em>, 1766-1778.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-50 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042796_0011-300x100.jpeg\" alt=\"\" width=\"426\" height=\"142\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042796_0011-300x100.jpeg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042796_0011-768x257.jpeg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042796_0011-1024x342.jpeg 1024w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042796_0011-604x202.jpeg 604w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042796_0011-100x33.jpeg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042796_0011.jpeg 1050w\" sizes=\"auto, (max-width: 426px) 85vw, 426px\" \/><\/p>\n<p>30. Toro-Vazquez, J. F.; Morales-Rueda, J.; Martinez, A. T.; Alonso,\u00a0M. A. C.;\u00a0 <strong>Mallia,\u00a0V. A<\/strong>.;\u00a0 Weiss, R. G.\u00a0 Cooling rate effects on the microstructure, solid content and rheological properties of organogels of amides derived from stearic acid and (R)-12-hydroxystearic acid in vegetable oil.<br \/>\n<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/la400809a\"><em>Langmuir<\/em><\/a>,\u00a0<strong>2013<\/strong>, <em>29<\/em>, 7642-7654.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-51 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00809a_0005-300x217.jpeg\" alt=\"\" width=\"263\" height=\"190\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00809a_0005-300x217.jpeg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00809a_0005-768x556.jpeg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00809a_0005-373x270.jpeg 373w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00809a_0005-100x72.jpeg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2013-00809a_0005.jpeg 774w\" sizes=\"auto, (max-width: 263px) 85vw, 263px\" \/><\/p>\n<p>29.<strong> Mallia,\u00a0V. A<\/strong>.; Butler, P. D.; Sarkar, B.; Holman, K. T.; \u00a0Weiss, R. G. Reversible phase transitions within self-assembled fibrillar networks of (R)-18-(n-alkylamino)octadecan-7-ols in their carbon tetrachloride gels <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja204371b\"><em>J. Am. Chem. Soc. <\/em><\/a><strong>2011<\/strong>, <em>133<\/em>, 15045-15054.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-68 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jacsat_v133i038-226x300.jpg\" alt=\"\" width=\"284\" height=\"376\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jacsat_v133i038-226x300.jpg 226w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jacsat_v133i038-768x1020.jpg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jacsat_v133i038-771x1024.jpg 771w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jacsat_v133i038-203x270.jpg 203w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jacsat_v133i038-75x100.jpg 75w\" sizes=\"auto, (max-width: 284px) 85vw, 284px\" \/><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-53 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/ja-2011-04371b_0013-300x131.jpeg\" alt=\"\" width=\"581\" height=\"254\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/ja-2011-04371b_0013-300x131.jpeg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/ja-2011-04371b_0013-768x336.jpeg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/ja-2011-04371b_0013-604x264.jpeg 604w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/ja-2011-04371b_0013-100x44.jpeg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/ja-2011-04371b_0013.jpeg 946w\" sizes=\"auto, (max-width: 581px) 85vw, 581px\" \/><\/p>\n<p>28.<strong> Mallia, V. A.<\/strong>; Terech, P.; Weiss R. G. Correlations of properties and structures at different length scales of hydro- and organogels based on <em>N<\/em>-alkyl-<em>(R)<\/em>-12-hydroxyoctadecylammonium chlorides. <em><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jp207182p\">J. Phys. Chem. B<\/a> <\/em><strong>2011<\/strong>, <em>115<\/em>, 12401-12414.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-54 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jp-2011-07182p_0010-300x117.jpeg\" alt=\"\" width=\"444\" height=\"173\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jp-2011-07182p_0010-300x117.jpeg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jp-2011-07182p_0010-768x300.jpeg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jp-2011-07182p_0010-1024x400.jpeg 1024w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jp-2011-07182p_0010-604x236.jpeg 604w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jp-2011-07182p_0010-100x39.jpeg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/jp-2011-07182p_0010.jpeg 2000w\" sizes=\"auto, (max-width: 444px) 85vw, 444px\" \/><\/p>\n<p>27.Toro-Vazquez, J. F.; Morales-Rueda, J.; <strong>Mallia,\u00a0V. A<\/strong>.; Weiss, R. G. Relation between molecular structure and thermo mechanical properties of\u00a0 candelilla wax and amides derived from (R)-12-hydroxystearic acid as gelators for safflower oil. <em><a href=\"https:\/\/link.springer.com\/article\/10.1007\/s11483-010-9159-y\">Food Biophys<\/a>. <\/em><strong>2010<\/strong>, <em>5<\/em>, 193-202.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/static-content.springer.com\/cover\/journal\/11483\/5\/3.jpg\" alt=\"Food Biophysics\" width=\"217\" height=\"287\" \/><\/p>\n<p>26. <strong>Mallia, V. A<\/strong>.; George, M.; Blair, D.; Weiss, R. G. Robust organogels from nitrogen-containing derivatives of (R)-12-hydroxystearic acid as gelators: comparisons with gels from stearic acid derivatives. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/la8042439\"><em>Langmuir<\/em><\/a> <strong>2009<\/strong>, <em>25<\/em>, 8615-8625.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-57 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042439_0003-300x117.jpeg\" alt=\"\" width=\"377\" height=\"147\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042439_0003-300x117.jpeg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042439_0003-768x301.jpeg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042439_0003-1024x401.jpeg 1024w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042439_0003-604x236.jpeg 604w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042439_0003-100x39.jpeg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2008-042439_0003.jpeg 1050w\" sizes=\"auto, (max-width: 377px) 85vw, 377px\" \/><\/p>\n<p>25. Bag, B. G.; Dinda, S. K.; Dey, P. P.; <strong>Mallia, V. A.<\/strong>; Weiss, R. G. Self-assembly of esters of arjunolic acid into fibrous networks and the properties of their organogels.<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/la8042796\"> <em>Langmuir<\/em><\/a> <strong>2009<\/strong>, <em>25<\/em>, 8663-8671.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-69 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cover.jpg\" alt=\"\" width=\"328\" height=\"437\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cover.jpg 115w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cover-75x100.jpg 75w\" sizes=\"auto, (max-width: 328px) 85vw, 328px\" \/><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-56 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2012-04485e_0013-300x122.jpeg\" alt=\"\" width=\"501\" height=\"204\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2012-04485e_0013-300x122.jpeg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2012-04485e_0013-768x313.jpeg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2012-04485e_0013-604x246.jpeg 604w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2012-04485e_0013-100x41.jpeg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/la-2012-04485e_0013.jpeg 1000w\" sizes=\"auto, (max-width: 501px) 85vw, 501px\" \/><\/p>\n<p>24.<strong> Mallia V. A<\/strong>.; Vemula, P. K.; John, G.; Kumar, A.; Ajayan, P. M. In situ synthesis and assembly of gold nanoparticles embedded in glass forming liquid crystals. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ange.200604218\/full\"><em>Angew. Chem. Int. Ed. <\/em><\/a><strong>2007<\/strong>, <em>46<\/em>, 3269-3274.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-132 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/angew.gif\" alt=\"\" width=\"408\" height=\"208\" \/><\/p>\n<p>23.<strong> Mallia, V. A<\/strong>.; Funahashi, M.; Tamaoki, N. Study of unsymmetrical dimesogens containing 4-heptylazobenzene.<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/poc.1231\/full\"> <em>J. Phys. Org. Chem. <\/em><\/a><strong>2007<\/strong>, <em>20<\/em>, 878-883.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/wol-prod-cdn.literatumonline.com\/cms\/attachment\/5f878420-ba71-4e49-bc39-19eb367dccc1\/mgra001.jpg\" width=\"582\" height=\"158\" \/><\/p>\n<p>22. Vemula, P. K.; <strong>Mallia V. A<\/strong>.; Bizati, K.; John, G. Cholesterol phenoxy hexanoate mesogens: effect of lateral substituents on their liquid crystalline behavior and in situ metal nanoparticle synthesis. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm071359q\"><em>Chem. Mater. <\/em><\/a><strong>2007<\/strong>, <em>19<\/em>, 5203-5206.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-133 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm071359qn00001-300x170.gif\" alt=\"\" width=\"401\" height=\"227\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm071359qn00001-300x170.gif 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm071359qn00001-476x270.gif 476w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm071359qn00001-100x57.gif 100w\" sizes=\"auto, (max-width: 401px) 85vw, 401px\" \/><\/p>\n<p>21. Vemula, P. K.; <strong>Mallia V. A<\/strong>.; Aslam, U..; John, G. \u201cIn situ synthesis of gold nanoparticles using molecular gels and liquid crystals from vitamin-C amphiphiles. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm062464n\"><em>Chem. Mater. <\/em><\/a><strong>2007<\/strong>, <em>19<\/em>, 138-140.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-135 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm062464nn00001-300x213.gif\" alt=\"\" width=\"369\" height=\"262\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm062464nn00001-300x213.gif 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm062464nn00001-380x270.gif 380w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm062464nn00001-100x71.gif 100w\" sizes=\"auto, (max-width: 369px) 85vw, 369px\" \/><\/p>\n<p>20. Abraham, S.; <strong>Mallia, V. A.<\/strong>; Rateesh, K. V.; Tamaoki, N.; Das, S. Reversible thermal and photochemical switching of liquid crystalline phases and luminescence in diphenyl butadiene-based mesogenic dimers. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja061575k\"><em>J. Am. Chem. Soc. <\/em><\/a><strong>2006<\/strong>, <em>128<\/em>, 7692-7698.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-137 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/ja061575kn00001-300x139.gif\" alt=\"\" width=\"409\" height=\"190\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/ja061575kn00001-300x139.gif 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/ja061575kn00001-100x46.gif 100w\" sizes=\"auto, (max-width: 409px) 85vw, 409px\" \/><\/p>\n<p>19. Akiyama, H.; <strong>Mallia, V. A.<\/strong>; Tamaoki, N. Novel photoresponsive oligomeric mesogens: synthesis, liquid crystalline properties and photo optical studies as a dopant in a chiral glassy liquid crystal. <em><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adfm.200500176\/full\">Adv. Funct. Mater.<\/a> <\/em><strong>2006<\/strong>, <em>16<\/em>, 477-484.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-139 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/mcontent.gif\" alt=\"\" width=\"318\" height=\"316\" \/><\/p>\n<p>18. Mallia, V. A.; Tamaoki, N. Study of chiral dimesogens: liquid crystalline properties, effect of smectic cybotactic domains in controlling the chiral reflections and glassy liquid crystal forming properties.<em><a href=\"http:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/15421400600654132\"> Mol. Cryst. Liq. Cryst.<\/a> <\/em>2006, <em>454<\/em>, 81-90.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/www.tandfonline.com\/na101\/home\/literatum\/publisher\/tandf\/journals\/content\/gmcl20\/2017\/gmcl20.v656.i01\/gmcl20.v656.i01\/20171214-01\/gmcl20.v656.i01.cover.jpg\" alt=\"Publication Cover\" width=\"183\" height=\"262\" \/><\/p>\n<p>17. Kumaresan, S.; Mallia, V. A.; Tamaoki, N. Thermal and photooptical properties of azoxybenzene\/alkyloxy azobenzene\u2013cholesterol with alkyl diacetylene linker containing dimesogens. <em><a href=\"https:\/\/www.cambridge.org\/core\/journals\/journal-of-materials-research\/article\/div-classtitlethermal-and-photo-optical-properties-of-azoxybenzenealkyloxy-azobenzenecholesterol-dimesogens-with-alkyl-diacetylene-linkerdiv\/17EB1EBD13AD05F9F9C4DBE3FC199DCE\">J. Mater. Res.<\/a> <\/em>2005, <em>20<\/em>, 3431-3438.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/static.cambridge.org\/covers\/JMR_0_20_12\/cover.jpg?send-default-cover=false\" alt=\"Journal of Materials Research Volume 20 - Issue 12 -\" width=\"185\" height=\"244\" \/><\/p>\n<p>16.<strong> Mallia, V. A.; <\/strong>Tamaoki, N. Photoactive dimesogen having different pathways of light driven phase transitions at different temperatures. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2004\/cc\/b410902c\/unauth#!divAbstract\"><em>Chem. Commun.<\/em><\/a> <strong>2004<\/strong>, 2538-2539.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/pubs.rsc.org\/en\/Image\/Get?imageInfo.ImageType=GA&amp;imageInfo.ImageIdentifier.ManuscriptID=B410902C\" alt=\"Graphical abstract: Photoactive dimesogen having different pathways of light driven phase transitions at different temperatures\" width=\"502\" height=\"182\" \/><\/p>\n<p>15.<strong> Mallia, V. A<\/strong>.<strong>; <\/strong>Tamaoki, N. Design of chiral dimesogens forming new molecular organizations and their application to molecular photonics. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2004\/cs\/b106617j\/unauth#!divAbstract\"><em>Chem. Soc. Rev. <\/em><\/a><strong>2004<\/strong>, <em>33<\/em>, 76-84.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/pubs.rsc.org\/en\/Image\/Get?imageInfo.ImageType=CoverIssue&amp;imageInfo.ImageIdentifier.SerCode=CS&amp;imageInfo.ImageIdentifier.IssueId=CS033002\" width=\"277\" height=\"363\" \/><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/pubs.rsc.org\/en\/Image\/Get?imageInfo.ImageType=GA&amp;imageInfo.ImageIdentifier.ManuscriptID=B106617J\" alt=\"Graphical abstract: Design of chiral dimesogens containing cholesteryl groups; formation of new molecular organizations and their application to molecular photonics\" width=\"475\" height=\"231\" \/><\/p>\n<p>14. Matsumoto, M.; Nakazawa, T.; <strong>Mallia, V. A.<\/strong>; Tamaoki, N.; Azumi, R.; Sakai, H.; Abe, M. Hysteresis in photoresponsivity of langmuir film of amphiphilic spiropyran. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja038844g\"><em>J. Am. Chem. Soc. <\/em><\/a><strong>2004<\/strong>, <em>126<\/em>, 1006-1007.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-814 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ja038844gn00001-300x105.jpeg\" alt=\"\" width=\"686\" height=\"240\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ja038844gn00001-300x105.jpeg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ja038844gn00001-768x270.jpeg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ja038844gn00001-1024x360.jpeg 1024w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ja038844gn00001-100x35.jpeg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/ja038844gn00001.jpeg 1050w\" sizes=\"auto, (max-width: 686px) 85vw, 686px\" \/><\/p>\n<p>13. Davis, R.; <strong>Mallia, V. A.<\/strong>; Das, S.; Tamaoki, N. Butadienes as novel photochromes for color tuning of cholesteric glasses: influence of microscopic molecular reorganization within the helical super structure. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adfm.200305190\/full\">Adv. Funct. Mater.<\/a> <strong>2004<\/strong>, 14, 743-748.<\/p>\n<p>12.<strong> Mallia, V. A.<\/strong>; Tamaoki, N. Photo-thermal effects of some cholesterol azobenzene containing dimesogens. <a href=\"https:\/\/www.mrs-j.org\/pub\/tmrsj\/cont29-7.pdf\"><em>Trans. Mater. Res. Soc. Jpn.<\/em><\/a> <strong>2004<\/strong>, 29, 3123-3125.<\/p>\n<p>11. Antharjanam, P. K. S.; <strong>Mallia, V. A<\/strong>.; Das, S. Synthesis and study of novel azopyridine containing hexacatenar silver mesogens. <a href=\"http:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/02678290410001675138\">Liq. Cryst.<\/a> <strong>2004<\/strong>, 31, 713-717.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/www.tandfonline.com\/na101\/home\/literatum\/publisher\/tandf\/journals\/content\/tlct20\/2017\/tlct20.v044.i14-15\/tlct20.v044.i14-15\/20171217-01\/tlct20.v044.i14-15.cover.jpg\" alt=\"Publication Cover\" width=\"187\" height=\"244\" \/><\/p>\n<p>10.\u00a0<strong>Mallia, V. A.<\/strong>; Tamaoki, N. Photochemically driven smectic-cholesteric phase transition in an inherently photoactive dimesogen. <em><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm034127%2B?journalCode=cmatex\">Chem. Mater.<\/a> <\/em><strong>2003<\/strong>, <em>15<\/em>, 3237-3239.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-145 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm0341271n00001-300x222.gif\" alt=\"\" width=\"223\" height=\"165\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm0341271n00001-300x222.gif 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm0341271n00001-365x270.gif 365w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm0341271n00001-100x74.gif 100w\" sizes=\"auto, (max-width: 223px) 85vw, 223px\" \/><\/p>\n<p>9.<strong> Mallia, V. A.<\/strong>; Tamaoki, N. Photoresponsive vitrifiable chiral dimesogens: photo-thermal modulation of microscopic disordering in helical superstructure and glass-forming properties. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2003\/jm\/b210541a\/unauth#!divAbstract\">J. Mater. Chem.<\/a> <strong>2003<\/strong>, 13, 219-224.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/pubs.rsc.org\/en\/Image\/Get?imageInfo.ImageType=GA&amp;imageInfo.ImageIdentifier.ManuscriptID=B210541A\" alt=\"Graphical abstract: Photoresponsive vitrifiable chiral dimesogens: photo-thermal modulation of microscopic disordering in helical superstructure and glass-forming properties\" width=\"351\" height=\"151\" \/><\/p>\n<p>8. Davis, R.; <strong>Mallia, V. A.<\/strong>; Das, S. Reversible photochemical phase transition behaviour of alkoxy-cyano-substituted diphenylbutadiene liquid crystals. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm020710z\">Chem. Mater.<\/a> <strong>2003<\/strong>, 15, 1057-1063.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-816 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-butadiene-300x80.jpg\" alt=\"\" width=\"705\" height=\"188\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-butadiene-300x80.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-butadiene-768x204.jpg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-butadiene-1024x272.jpg 1024w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-butadiene-1200x318.jpg 1200w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-butadiene-100x27.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-butadiene.jpg 1244w\" sizes=\"auto, (max-width: 705px) 85vw, 705px\" \/><\/p>\n<p>7. Takahashi, A.; <strong>Mallia, V. A.<\/strong>; Tamaoki, N. Novel supramolecular hydrogen-bonded cholesteric mesogens: liquid crystalline, thermoptical and glass-forming properties. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2003\/jm\/b302198j\/unauth#!divAbstract\">J. Mater. Chem.<\/a> <strong>2003<\/strong>, 13, 1582-1587.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/pubs.rsc.org\/en\/Image\/Get?imageInfo.ImageType=GA&amp;imageInfo.ImageIdentifier.ManuscriptID=B302198J\" alt=\"Graphical abstract: Novel supramolecular hydrogen-bonded cholesteric mesogens: liquid crystalline, thermoptical and glass-forming properties\" width=\"460\" height=\"94\" \/><\/p>\n<p>6.<strong> Mallia, V. A.<\/strong>; Antharjanam, P. K. S.; Das, S. Synthesis and studies of some substituted 4-phenyl, 4&#8242;-azopyridine containing hydrogen bonded supramolecular mesogens. <a href=\"http:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/02678290010006315\"><em>Liq. Cryst. <\/em><\/a><strong>2003<\/strong>, <em>30<\/em>, 135-141.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/www.tandfonline.com\/na101\/home\/literatum\/publisher\/tandf\/journals\/content\/tlct20\/2017\/tlct20.v044.i14-15\/tlct20.v044.i14-15\/20171217-01\/tlct20.v044.i14-15.cover.jpg\" alt=\"Publication Cover\" width=\"216\" height=\"282\" \/><\/p>\n<p>5. Antharjanam, P. K. S.; <strong>Mallia, V. A.<\/strong>; Das, S. Novel azopyridine-containing silver mesogens; synthesis, liquid crystalline and photophysical properties. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm011730o\">Chem. Mater.<\/a> <strong>2002<\/strong>, 14, 2687-2692.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-150 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2018\/01\/cm011730of00001.gif\" alt=\"\" width=\"271\" height=\"655\" \/>\u00a04.\u00a0<strong>Mallia, V. A.<\/strong>; Antharjanam, P. K. S.; Das, S. Chiral nematic glasses from novel hydrogen bonded mesogens. <a href=\"http:\/\/www.journal.csj.jp\/doi\/abs\/10.1246\/cl.2001.752\"><em>Chem. Lett. <\/em><\/a><strong>2001<\/strong>, 752-753.<\/p>\n<p>3.<strong> Mallia, V. A.<\/strong>; Das, S. Synthesis and studies of some cholest-5-en-3-ol-(3b)[4-phenyl- pyridyl-azo]carbonate containing supra-molecular hydrogen bonded mesogens. <em><a href=\"http:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/02678290010006315\">Liq. Cryst<\/a>. <\/em><strong>2001<\/strong>, <em>28<\/em>, 259-264.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/www.tandfonline.com\/na101\/home\/literatum\/publisher\/tandf\/journals\/content\/tlct20\/2017\/tlct20.v044.i14-15\/tlct20.v044.i14-15\/20171217-01\/tlct20.v044.i14-15.cover.jpg\" alt=\"Publication Cover\" width=\"219\" height=\"286\" \/><\/p>\n<p>2. George, M.; <strong>Mallia, V. A.<\/strong>; Antharjanam, P. K. S.; Saminathan, M.; Das, S. Synthesis and studies of some cholesterol containing liquid crystals. <a href=\"http:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/10587250008025238\">Mol. Cryst. Liq. Cryst.<\/a> <strong>2000<\/strong>, 350, 125-139.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"http:\/\/www.tandfonline.com\/na101\/home\/literatum\/publisher\/tandf\/journals\/content\/gmcl20\/2017\/gmcl20.v656.i01\/gmcl20.v656.i01\/20171214-01\/gmcl20.v656.i01.cover.jpg\" alt=\"Publication Cover\" width=\"222\" height=\"318\" \/><\/p>\n<ol>\n<li><strong>Mallia, V. A.<\/strong>; George, M.; Das, S. Photochemical phase transition in hydrogen bonded liquid crystals. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm980455b\"><em>Chem. Mater. <\/em><\/a><strong>1999<\/strong>, <em>11<\/em>, 207-208.<\/li>\n<\/ol>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-811 aligncenter\" src=\"http:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-300x98.jpg\" alt=\"\" width=\"686\" height=\"224\" srcset=\"https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-300x98.jpg 300w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-768x250.jpg 768w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-1024x333.jpg 1024w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater-100x33.jpg 100w, https:\/\/commons.ggc.edu\/amallia\/wp-content\/uploads\/sites\/39\/2020\/08\/chem-mater.jpg 1106w\" sizes=\"auto, (max-width: 686px) 85vw, 686px\" \/><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Undergraduate co-authors are underlined and high school students are italicized. 46. Mallia, A.; Sloop, J. Advances in the Synthesis of Heteroaromatic Hybrid Chalcones. Molecules 2023, 28(7), 3201; https:\/\/doi.org\/10.3390\/molecules28073201 45. Faass, M.; Mallia, A.; Sommer, R., Sloop, J. (Z)-2-(3, 5-Dimethoxybenzylidene) Indan-1-one. CCDC 2081969: Experimental Crystal Structure Determination. CSD Communication, 2021, DOI: 10.5517\/ccdc.csd.cc27wg9x. 44. Boyle, P., Breaud, &hellip; <a href=\"https:\/\/commons.ggc.edu\/amallia\/publications\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Publications&#8221;<\/span><\/a><\/p>\n","protected":false},"author":41,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_exactmetrics_skip_tracking":false,"_exactmetrics_sitenote_active":false,"_exactmetrics_sitenote_note":"","_exactmetrics_sitenote_category":0,"footnotes":""},"class_list":["post-32","page","type-page","status-publish","hentry","user-has-not-earned"],"_links":{"self":[{"href":"https:\/\/commons.ggc.edu\/amallia\/wp-json\/wp\/v2\/pages\/32","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/commons.ggc.edu\/amallia\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/commons.ggc.edu\/amallia\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/commons.ggc.edu\/amallia\/wp-json\/wp\/v2\/users\/41"}],"replies":[{"embeddable":true,"href":"https:\/\/commons.ggc.edu\/amallia\/wp-json\/wp\/v2\/comments?post=32"}],"version-history":[{"count":0,"href":"https:\/\/commons.ggc.edu\/amallia\/wp-json\/wp\/v2\/pages\/32\/revisions"}],"wp:attachment":[{"href":"https:\/\/commons.ggc.edu\/amallia\/wp-json\/wp\/v2\/media?parent=32"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}