{"id":1037,"date":"2019-01-28T03:19:54","date_gmt":"2019-01-28T08:19:54","guid":{"rendered":"http:\/\/www.bocsci.com\/blog\/?p=1037"},"modified":"2019-01-28T03:34:45","modified_gmt":"2019-01-28T08:34:45","slug":"cens-molecules-of-the-year-for-2018","status":"publish","type":"post","link":"https:\/\/www.bocsci.com\/blog\/cens-molecules-of-the-year-for-2018\/","title":{"rendered":"C&#038;EN\u2019s molecules of the year for 2018"},"content":{"rendered":"<p>The US journal Chemical and Chemical News (C&amp;EN) recently published its 2018 Molecular list. These molecules received a lot of attention in 2018. Let\u2019s take a look at these attractive chemical molecules.<br \/>\nThe first new stereoisomer (stereoisomers) discovered in half a century.<br \/>\nIn the synthesis of porphyrin macrocyclic (porphyrin macrocycles) containing a boron-oxo-boron bridge, a new isomer was discovered by an international research team. In this macrocyclic porphyrin molecule, the oxygen atoms in the boron-oxygen-boron bridge can move from one side of the porphyrin ring to the other side.<\/p>\n<p><a href=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/The-first-new-stereoisomer.png\"><img decoding=\"async\" loading=\"lazy\" class=\"size-medium wp-image-1038 aligncenter\" src=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/The-first-new-stereoisomer-300x255.png\" alt=\"\" width=\"300\" height=\"255\" srcset=\"https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/The-first-new-stereoisomer-300x255.png 300w, https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/The-first-new-stereoisomer.png 450w\" sizes=\"(max-width: 300px) 100vw, 300px\" \/><\/a><\/p>\n<p><strong>Russian nerve agent found in Britain. <\/strong><\/p>\n<p>The case of a Russian double agent and his daughter who lived in Salisbury, England, has made headlines this year, and the nerve agent that tried to kill them is Novichok, which is a kind of nerve agents and called A-234.<\/p>\n<p><a href=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/A-234.png\"><img decoding=\"async\" loading=\"lazy\" class=\"size-medium wp-image-1039 aligncenter\" src=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/A-234-300x200.png\" alt=\"\" width=\"300\" height=\"200\" srcset=\"https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/A-234-300x200.png 300w, https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/A-234.png 525w\" sizes=\"(max-width: 300px) 100vw, 300px\" \/><\/a><\/p>\n<p><strong>Graphene with nanopores.<\/strong><\/p>\n<p>Scientists in Spain used chemical synthesis to synthesize graphene, which appears in an array of nanopores at a specific location. This synthesis method can control the size, density, shape and chemical composition of the nanopores in the atomic-level precision. The graphene materials formed have semiconductor properties and can be used in the manufacture of semiconductor materials or in molecular sieve separation and sensing.<\/p>\n<p><a href=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Graphene-with-nanopores-1.png\"><img decoding=\"async\" loading=\"lazy\" class=\" wp-image-1059 aligncenter\" src=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Graphene-with-nanopores-1-297x300.png\" alt=\"\" width=\"404\" height=\"408\" srcset=\"https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Graphene-with-nanopores-1-297x300.png 297w, https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Graphene-with-nanopores-1-150x150.png 150w, https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Graphene-with-nanopores-1.png 563w\" sizes=\"(max-width: 404px) 100vw, 404px\" \/><\/a><\/p>\n<p><strong>Dimethyl calcium, which seems simple but difficult to synthesize. <\/strong><\/p>\n<p>Scientists first announced the synthesis of dimethylcalcium, more than 60 years ago, but the synthesis has not been replicated since. Until this year, German scientists published a paper that successfully synthesized this seemingly simple molecule again. This may lead to new catalysts and chemical reagents. The key to synthesis is to find the right starting material and devise a way to purify highly contaminated reactants. The researchers used dimethyl calcium to prepare the double Grignard reagent (heavy Grignard reagent) and the terminal calcium methyl compounds.<\/p>\n<p><a href=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Dimethyl-calcium-1.png\"><img decoding=\"async\" loading=\"lazy\" class=\" wp-image-1052 aligncenter\" src=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Dimethyl-calcium-1-300x112.png\" alt=\"\" width=\"544\" height=\"203\" srcset=\"https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Dimethyl-calcium-1-300x112.png 300w, https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Dimethyl-calcium-1.png 597w\" sizes=\"(max-width: 544px) 100vw, 544px\" \/><\/a><\/p>\n<p><strong>A supermolecular comp<\/strong><strong>lex resembling Saturn\u2019s rings. <\/strong><\/p>\n<p>Chemists at (Tokyo Institute of Technology) Tokyo Polytechnic University in Japan have built a supermolecular complex like Saturn\u2019s nanoscale. It binds a C60 to a large hydrocarbon ring made up of substituted anthracene units. The weak CH- \u03c0 forces bind the entire complex together.<\/p>\n<p><strong>Synthetic Deathcap Mushroom toxin. <\/strong><\/p>\n<p>Researchers at (University of British Columbia) University of British Columbia in Canada have found a way to chemically synthesize \u03b1-amanitin. It\u2019s a toxin produced by poisonous mushrooms called death caps, and it may be a potential anticancer compound.<\/p>\n<p><strong>Molecular knots produced by chemists. <\/strong><\/p>\n<p>Chemists at the University of Manchester, United Kingdom, have linked six precursor molecules together to form one of the world\u2019s most complex molecular knots to date. The molecular junction is made up of a 324-atom molecular ring, which contains nine crossing points. Although the synthesis of these molecular junctions is currently seen as a demonstration of the power of chemical synthesis, researchers hope that they can be used as catalysts or other applications in the future.<\/p>\n<p><a href=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Molecular-knots-produced-by-chemists.png\"><img decoding=\"async\" loading=\"lazy\" class=\"size-medium wp-image-1054 aligncenter\" src=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Molecular-knots-produced-by-chemists-287x300.png\" alt=\"\" width=\"287\" height=\"300\" srcset=\"https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Molecular-knots-produced-by-chemists-287x300.png 287w, https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Molecular-knots-produced-by-chemists.png 542w\" sizes=\"(max-width: 287px) 100vw, 287px\" \/><\/a><\/p>\n<p><strong>Free radical Polymer with Electrical conductivity record Breaking<\/strong><\/p>\n<p>Free radical polymers are generally less conductive than conjugated polymers. However, researchers at Purdue University have synthesized a new type of non-conjugated organic free radical polymer, which is more than 1000 times more conductive than other organic free radical polymers. The material may be integrated into a battery or display.<\/p>\n<p><a href=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Free-radical-Polymer-with-Electrical-conductivity-record-Breaking.png\"><img decoding=\"async\" loading=\"lazy\" class=\"size-medium wp-image-1056 aligncenter\" src=\"http:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Free-radical-Polymer-with-Electrical-conductivity-record-Breaking-155x300.png\" alt=\"\" width=\"155\" height=\"300\" srcset=\"https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Free-radical-Polymer-with-Electrical-conductivity-record-Breaking-155x300.png 155w, https:\/\/www.bocsci.com\/blog\/wp-content\/uploads\/2019\/01\/Free-radical-Polymer-with-Electrical-conductivity-record-Breaking.png 234w\" sizes=\"(max-width: 155px) 100vw, 155px\" \/><\/a><\/p>\n<p>References<\/p>\n<p>1. Canfield, P. J., Blake, I. M., Cai, Z. L., Luck, I. J., Krausz, E., Kobayashi, R., &#8230; &amp; Crossley, M. J. (2018). A new fundamental type of conformational isomerism.\u00a0<em>Nature chemistry<\/em>,\u00a0<em>10<\/em>(6), 615.<\/p>\n<p>2. Moreno, C., Vilas-Varela, M., Kretz, B., Garcia-Lekue, A., Costache, M. V., Paradinas, M., &#8230; &amp; Mugarza, A. (2018). Bottom-up synthesis of multifunctional nanoporous graphene.\u00a0<em>Science<\/em>,\u00a0<em>360<\/em>(6385), 199-203.<\/p>\n<p>3. Wolf, B. M., Stuhl, C., Maichle-Mo\u0308ssmer, C., &amp; Anwander, R. (2018). Dimethylcalcium.\u00a0<em>Journal of the American Chemical Society<\/em>,\u00a0<em>140<\/em>(6), 2373-2383.<\/p>\n<p>4. Yamamoto, Y., Tsurumaki, E., Wakamatsu, K., &amp; Toyota, S. (2018). Nano\u2010Saturn: Experimental Evidence of Complex Formation of an Anthracene Cyclic Ring with C60.\u00a0<em>Angewandte Chemie International Edition<\/em>.<\/p>\n<p>5. Matinkhoo, K., Pryyma, A., Todorovic, M., Patrick, B. O., &amp; Perrin, D. M. (2018). Synthesis of the death-cap mushroom toxin \u03b1-amanitin.\u00a0<em>Journal of the American Chemical Society<\/em>,\u00a0<em>140<\/em>(21), 6513-6517.<\/p>\n<p>6. Zhang, L., Stephens, A. J., Nussbaumer, A. L., Lemonnier, J. F., Jur\u010dek, P., Vitorica-Yrezabal, I. J., &amp; Leigh, D. A. (2018). Stereoselective synthesis of a composite knot with nine crossings.\u00a0<em>Nature chemistry<\/em>,\u00a0<em>10<\/em>(11), 1083.<\/p>\n<p>7. Joo, Y., Agarkar, V., Sung, S. H., Savoie, B. M., &amp; Boudouris, B. W. (2018). A nonconjugated radical polymer glass with high electrical conductivity.\u00a0<em>Science<\/em>,\u00a0<em>359<\/em>(6382), 1391-1395.<\/p>\n<p><strong>Related Products and Services<\/strong><\/p>\n<p><a href=\"https:\/\/www.bocsci.com\/superparamagnetic-iron-oxide-nano.html\">Superparamagnetic Iron Oxide Nano\/Micro Particles Preparation<\/a><\/p>\n<p><a href=\"https:\/\/www.bocsci.com\/search?q=polymer\">polymer<\/a>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 \u00a0<a href=\"https:\/\/www.bocsci.com\/amanitin-cas-11030-71-0-item-82778.html\">\u03b1-amanitin<\/a><\/p>\n<p><a href=\"https:\/\/www.bocsci.com\/search?q=Free%20radical&amp;page=1\">Free radical<\/a>\u00a0\u00a0\u00a0 \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0<a href=\"https:\/\/www.bocsci.com\/search?q=stereoisomer\">Stereoisomer<\/a><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The US journal Chemical and Chemical News (C&amp;EN) recently published its 2018 Molecular list. These molecules received a lot of attention in 2018. Let\u2019s take a look at these attractive [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[20],"tags":[],"_links":{"self":[{"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/posts\/1037"}],"collection":[{"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/comments?post=1037"}],"version-history":[{"count":5,"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/posts\/1037\/revisions"}],"predecessor-version":[{"id":1047,"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/posts\/1037\/revisions\/1047"}],"wp:attachment":[{"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/media?parent=1037"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/categories?post=1037"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.bocsci.com\/blog\/wp-json\/wp\/v2\/tags?post=1037"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}