<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Campbell E</submitter><funding>Research Councils UK</funding><pagination>6826-6834</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11229064</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(26)</volume><pubmed_abstract>Resonance Raman spectroscopy can provide insights into complex reaction mechanisms by selectively enhancing the signals of specific molecular species. In this work, we demonstrate that, by changing the excitation wavelength, Raman bands of different intermediates in the methanol-to-hydrocarbons reactions can be identified. We show in particular how UV excitation enhances signals from short-chain olefins and cyclopentadienyl cations during the induction period, while visible excitation better detects later-stage aromatics. However, visible excitation is prone to fluorescence that can obscure Raman signals, and hence, we show how fast fluorescence rejection techniques like Kerr gating are necessary for extracting useful information from visible excitation measurements.</pubmed_abstract><journal>The journal of physical chemistry letters</journal><pubmed_title>Methanol-to-Olefins Studied by UV Raman Spectroscopy as Compared to Visible Wavelength: Capitalization on Resonance Enhancement.</pubmed_title><pmcid>PMC11229064</pmcid><funding_grant_id>EP/K007467/1</funding_grant_id><funding_grant_id>EP/S016481/1</funding_grant_id><funding_grant_id>EP/R026815/1</funding_grant_id><pubmed_authors>Towrie M</pubmed_authors><pubmed_authors>Campbell E</pubmed_authors><pubmed_authors>Watson MJ</pubmed_authors><pubmed_authors>Lezcano-Gonzalez I</pubmed_authors><pubmed_authors>Sazanovich IV</pubmed_authors><pubmed_authors>Beale AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Methanol-to-Olefins Studied by UV Raman Spectroscopy as Compared to Visible Wavelength: Capitalization on Resonance Enhancement.</name><description>Resonance Raman spectroscopy can provide insights into complex reaction mechanisms by selectively enhancing the signals of specific molecular species. In this work, we demonstrate that, by changing the excitation wavelength, Raman bands of different intermediates in the methanol-to-hydrocarbons reactions can be identified. We show in particular how UV excitation enhances signals from short-chain olefins and cyclopentadienyl cations during the induction period, while visible excitation better detects later-stage aromatics. However, visible excitation is prone to fluorescence that can obscure Raman signals, and hence, we show how fast fluorescence rejection techniques like Kerr gating are necessary for extracting useful information from visible excitation measurements.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-04T11:24:41.842Z</modification><creation>2025-04-04T11:24:41.842Z</creation></dates><accession>S-EPMC11229064</accession><cross_references><pubmed>38916593</pubmed><doi>10.1021/acs.jpclett.4c00865</doi></cross_references></HashMap>