File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Time-Resolved Spectroscopic Study of N,N-Di(4-bromo)nitrenium Ions in Selected Solutions

TitleTime-Resolved Spectroscopic Study of N,N-Di(4-bromo)nitrenium Ions in Selected Solutions
Authors
Keywordsnitrenium ion
resonance Raman
transient absorption
reactive intermediate
Issue Date2018
PublisherMolecular Diversity Preservation International. The Journal's web site is located at http://www.mdpi.org/molecules
Citation
Molecules, 2018, v. 23 n. 12, p. article no. 3182 How to Cite?
AbstractNitrenium ions are important reactive intermediates in chemistry and biology. In this work, femtosecond and nanosecond transient absorption (fs-TA and ns-TA) along with nanosecond time-resolved resonance Raman (ns-TR3) experiments were employed to examine the photochemical pathways of N-(4,4-dibromodiphenylamino)-2,4,6-trimethylpyridinium BF4- (salt (DN) from just absorption of a photon of light to the production of the important N,N-di(4-bromophenyl)nitrenium ion 2. In acetonitrile (MeCN), the formation of halogenated diarylnitrenium ion 2 was observed within 4 ps, showing the vibrational spectra with strong intensity. The nucleophilic adduct reaction of ion 2 with H2O was also examined in aqueous solutions. The direct detection of the unique ortho adduct intermediate 3 shows that there is an efficient and exclusive reaction pathway for 2 with H2O. The results shown in this paper give new characterization of 2, which can be used to design time-resolved spectroscopy investigations of covalent addition reactions of nitrenium ions with other molecules in future studies.
Persistent Identifierhttp://hdl.handle.net/10722/273834
ISSN
2021 Impact Factor: 4.927
2020 SCImago Journal Rankings: 0.782
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorDu, L-
dc.contributor.authorLan, X-
dc.contributor.authorYan, Z-
dc.contributor.authorZhu, R-
dc.contributor.authorPhillips, DL-
dc.date.accessioned2019-08-18T14:49:30Z-
dc.date.available2019-08-18T14:49:30Z-
dc.date.issued2018-
dc.identifier.citationMolecules, 2018, v. 23 n. 12, p. article no. 3182-
dc.identifier.issn1420-3049-
dc.identifier.urihttp://hdl.handle.net/10722/273834-
dc.description.abstractNitrenium ions are important reactive intermediates in chemistry and biology. In this work, femtosecond and nanosecond transient absorption (fs-TA and ns-TA) along with nanosecond time-resolved resonance Raman (ns-TR3) experiments were employed to examine the photochemical pathways of N-(4,4-dibromodiphenylamino)-2,4,6-trimethylpyridinium BF4- (salt (DN) from just absorption of a photon of light to the production of the important N,N-di(4-bromophenyl)nitrenium ion 2. In acetonitrile (MeCN), the formation of halogenated diarylnitrenium ion 2 was observed within 4 ps, showing the vibrational spectra with strong intensity. The nucleophilic adduct reaction of ion 2 with H2O was also examined in aqueous solutions. The direct detection of the unique ortho adduct intermediate 3 shows that there is an efficient and exclusive reaction pathway for 2 with H2O. The results shown in this paper give new characterization of 2, which can be used to design time-resolved spectroscopy investigations of covalent addition reactions of nitrenium ions with other molecules in future studies.-
dc.languageeng-
dc.publisherMolecular Diversity Preservation International. The Journal's web site is located at http://www.mdpi.org/molecules-
dc.relation.ispartofMolecules-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectnitrenium ion-
dc.subjectresonance Raman-
dc.subjecttransient absorption-
dc.subjectreactive intermediate-
dc.titleTime-Resolved Spectroscopic Study of N,N-Di(4-bromo)nitrenium Ions in Selected Solutions-
dc.typeArticle-
dc.identifier.emailDu, L: ailleen@hku.hk-
dc.identifier.emailPhillips, DL: phillips@hku.hk-
dc.identifier.authorityPhillips, DL=rp00770-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3390/molecules23123182-
dc.identifier.pmid30513911-
dc.identifier.scopuseid_2-s2.0-85057587127-
dc.identifier.hkuros300966-
dc.identifier.volume23-
dc.identifier.issue12-
dc.identifier.spagearticle no. 3182-
dc.identifier.epagearticle no. 3182-
dc.identifier.isiWOS:000454523000132-
dc.publisher.placeSwitzerland-
dc.identifier.issnl1420-3049-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats