<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Anggara K</submitter><pubmed_abstract>Bond-selective reaction is central to heterogeneous catalysis. In heterogeneous catalysis, selectivity is found to depend on the chemical nature and morphology of the substrate. Here, however, we show a high degree of bond selectivity dependent only on adsorbate bond alignment. The system studied is the electron-induced reaction of meta-diiodobenzene physisorbed on Cu(110). Of the adsorbate's C-I bonds, C-I aligned 'Along' the copper row dissociates in 99.3% of the cases giving surface reaction, whereas C-I bond aligned 'Across' the rows dissociates in only 0.7% of the cases. A two-electronic-state molecular dynamics model attributes reaction to an initial transition to a repulsive state of an Along C-I, followed by directed recoil of C towards a Cu atom of the same row, forming C-Cu. A similar impulse on an Across C-I gives directed C that, moving across rows, does not encounter a Cu atom and hence exhibits markedly less reaction.</pubmed_abstract><journal>Nature communications</journal><pagination>13690</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5476794</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Bond selectivity in electron-induced reaction due to directed recoil on an anisotropic substrate.</pubmed_title><pmcid>PMC5476794</pmcid><pubmed_authors>Cheng F</pubmed_authors><pubmed_authors>Leung L</pubmed_authors><pubmed_authors>Polanyi JC</pubmed_authors><pubmed_authors>Huang K</pubmed_authors><pubmed_authors>Chatterjee A</pubmed_authors><pubmed_authors>Anggara K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bond selectivity in electron-induced reaction due to directed recoil on an anisotropic substrate.</name><description>Bond-selective reaction is central to heterogeneous catalysis. In heterogeneous catalysis, selectivity is found to depend on the chemical nature and morphology of the substrate. Here, however, we show a high degree of bond selectivity dependent only on adsorbate bond alignment. The system studied is the electron-induced reaction of meta-diiodobenzene physisorbed on Cu(110). Of the adsorbate's C-I bonds, C-I aligned 'Along' the copper row dissociates in 99.3% of the cases giving surface reaction, whereas C-I bond aligned 'Across' the rows dissociates in only 0.7% of the cases. A two-electronic-state molecular dynamics model attributes reaction to an initial transition to a repulsive state of an Along C-I, followed by directed recoil of C towards a Cu atom of the same row, forming C-Cu. A similar impulse on an Across C-I gives directed C that, moving across rows, does not encounter a Cu atom and hence exhibits markedly less reaction.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Dec</publication><modification>2021-03-18T08:15:05Z</modification><creation>2019-03-27T02:47:59Z</creation></dates><accession>S-EPMC5476794</accession><cross_references><pubmed>27934861</pubmed><doi>10.1038/ncomms13690</doi></cross_references></HashMap>