The hindering of the inversion motion in the van der Waals aniline-Arn clusters: An adiabatic molecular dynamics simulation for n=1–3

An adiabatic quantum molecular dynamics simulation has been performed for the van der Waals clusters aniline-Arn (with n=1–3) to understand the influence of the intramolecular inversion mode on the static properties (rotational constants). The effect of deuteration of the amino group in the chromoph...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of chemical physics 1998-02, Vol.108 (5), p.1932-1939
Hauptverfasser: Parneix, Pascal, Bréchignac, Philippe
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1939
container_issue 5
container_start_page 1932
container_title The Journal of chemical physics
container_volume 108
creator Parneix, Pascal
Bréchignac, Philippe
description An adiabatic quantum molecular dynamics simulation has been performed for the van der Waals clusters aniline-Arn (with n=1–3) to understand the influence of the intramolecular inversion mode on the static properties (rotational constants). The effect of deuteration of the amino group in the chromophore (C6H5NH2 or C6H5ND2) on the rotational constants of the complexes has been evaluated. The results are in good agreement with recent experimental values [W. E. Sinclair and D. W. Pratt, J. Chem. Phys. 105, 7942 (1996)]. In the ground electronic state S0, calculations show that the −NH2 (or −ND2) plane of the aniline molecule tends to be blocked on the same side as the argon atom in the complex. On the other hand, for larger clusters (aniline-Ar2 and aniline-Ar3), it appears that the −NH2 (or −ND2) group is more localized on the side opposite to the argon atoms for the isomers containing at least one argon atom bound in a site near the nitrogen atom.
doi_str_mv 10.1063/1.475573
format Article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1063_1_475573</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1063_1_475573</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1743-1a84ca53870deabd5814fde25cd5b8bf42fa857cbb778f2cf9aa1f384916d2a23</originalsourceid><addsrcrecordid>eNotkMtKAzEYhYMoWKvgI2TpZmquk4zgohRvILipuBz-ycVGZjKSTAvdufMBfEOfxGnr6sDHOd_iIHRJyYySkl_TmVBSKn6EJpToqlBlRY7RhBBGi6ok5Sk6y_mDEEIVExP0vVw5vArRuhTiO-49HkYQ4salHPqIu37YRYh7voGIxyZ-A2gzhhjaEF0xTxGbdp2HcXOD5xGDDdDAEMw4b51Zt5Cw3Ubogsk4h24Ee6vvE4639Pfrh5-jEz863cV_TtHr_d1y8Vg8vzw8LebPhaFK8IKCFgYk14pYB42VmgpvHZPGykY3XjAPWirTNEppz4yvAKjnWlS0tAwYn6Krg9ekPufkfP2ZQgdpW1NS7w6saX04kP8B1tdllQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The hindering of the inversion motion in the van der Waals aniline-Arn clusters: An adiabatic molecular dynamics simulation for n=1–3</title><source>AIP Digital Archive</source><creator>Parneix, Pascal ; Bréchignac, Philippe</creator><creatorcontrib>Parneix, Pascal ; Bréchignac, Philippe</creatorcontrib><description>An adiabatic quantum molecular dynamics simulation has been performed for the van der Waals clusters aniline-Arn (with n=1–3) to understand the influence of the intramolecular inversion mode on the static properties (rotational constants). The effect of deuteration of the amino group in the chromophore (C6H5NH2 or C6H5ND2) on the rotational constants of the complexes has been evaluated. The results are in good agreement with recent experimental values [W. E. Sinclair and D. W. Pratt, J. Chem. Phys. 105, 7942 (1996)]. In the ground electronic state S0, calculations show that the −NH2 (or −ND2) plane of the aniline molecule tends to be blocked on the same side as the argon atom in the complex. On the other hand, for larger clusters (aniline-Ar2 and aniline-Ar3), it appears that the −NH2 (or −ND2) group is more localized on the side opposite to the argon atoms for the isomers containing at least one argon atom bound in a site near the nitrogen atom.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.475573</identifier><language>eng</language><ispartof>The Journal of chemical physics, 1998-02, Vol.108 (5), p.1932-1939</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1743-1a84ca53870deabd5814fde25cd5b8bf42fa857cbb778f2cf9aa1f384916d2a23</citedby><cites>FETCH-LOGICAL-c1743-1a84ca53870deabd5814fde25cd5b8bf42fa857cbb778f2cf9aa1f384916d2a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids></links><search><creatorcontrib>Parneix, Pascal</creatorcontrib><creatorcontrib>Bréchignac, Philippe</creatorcontrib><title>The hindering of the inversion motion in the van der Waals aniline-Arn clusters: An adiabatic molecular dynamics simulation for n=1–3</title><title>The Journal of chemical physics</title><description>An adiabatic quantum molecular dynamics simulation has been performed for the van der Waals clusters aniline-Arn (with n=1–3) to understand the influence of the intramolecular inversion mode on the static properties (rotational constants). The effect of deuteration of the amino group in the chromophore (C6H5NH2 or C6H5ND2) on the rotational constants of the complexes has been evaluated. The results are in good agreement with recent experimental values [W. E. Sinclair and D. W. Pratt, J. Chem. Phys. 105, 7942 (1996)]. In the ground electronic state S0, calculations show that the −NH2 (or −ND2) plane of the aniline molecule tends to be blocked on the same side as the argon atom in the complex. On the other hand, for larger clusters (aniline-Ar2 and aniline-Ar3), it appears that the −NH2 (or −ND2) group is more localized on the side opposite to the argon atoms for the isomers containing at least one argon atom bound in a site near the nitrogen atom.</description><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNotkMtKAzEYhYMoWKvgI2TpZmquk4zgohRvILipuBz-ycVGZjKSTAvdufMBfEOfxGnr6sDHOd_iIHRJyYySkl_TmVBSKn6EJpToqlBlRY7RhBBGi6ok5Sk6y_mDEEIVExP0vVw5vArRuhTiO-49HkYQ4salHPqIu37YRYh7voGIxyZ-A2gzhhjaEF0xTxGbdp2HcXOD5xGDDdDAEMw4b51Zt5Cw3Ubogsk4h24Ee6vvE4639Pfrh5-jEz863cV_TtHr_d1y8Vg8vzw8LebPhaFK8IKCFgYk14pYB42VmgpvHZPGykY3XjAPWirTNEppz4yvAKjnWlS0tAwYn6Krg9ekPufkfP2ZQgdpW1NS7w6saX04kP8B1tdllQ</recordid><startdate>19980201</startdate><enddate>19980201</enddate><creator>Parneix, Pascal</creator><creator>Bréchignac, Philippe</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19980201</creationdate><title>The hindering of the inversion motion in the van der Waals aniline-Arn clusters: An adiabatic molecular dynamics simulation for n=1–3</title><author>Parneix, Pascal ; Bréchignac, Philippe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1743-1a84ca53870deabd5814fde25cd5b8bf42fa857cbb778f2cf9aa1f384916d2a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parneix, Pascal</creatorcontrib><creatorcontrib>Bréchignac, Philippe</creatorcontrib><collection>CrossRef</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parneix, Pascal</au><au>Bréchignac, Philippe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The hindering of the inversion motion in the van der Waals aniline-Arn clusters: An adiabatic molecular dynamics simulation for n=1–3</atitle><jtitle>The Journal of chemical physics</jtitle><date>1998-02-01</date><risdate>1998</risdate><volume>108</volume><issue>5</issue><spage>1932</spage><epage>1939</epage><pages>1932-1939</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><abstract>An adiabatic quantum molecular dynamics simulation has been performed for the van der Waals clusters aniline-Arn (with n=1–3) to understand the influence of the intramolecular inversion mode on the static properties (rotational constants). The effect of deuteration of the amino group in the chromophore (C6H5NH2 or C6H5ND2) on the rotational constants of the complexes has been evaluated. The results are in good agreement with recent experimental values [W. E. Sinclair and D. W. Pratt, J. Chem. Phys. 105, 7942 (1996)]. In the ground electronic state S0, calculations show that the −NH2 (or −ND2) plane of the aniline molecule tends to be blocked on the same side as the argon atom in the complex. On the other hand, for larger clusters (aniline-Ar2 and aniline-Ar3), it appears that the −NH2 (or −ND2) group is more localized on the side opposite to the argon atoms for the isomers containing at least one argon atom bound in a site near the nitrogen atom.</abstract><doi>10.1063/1.475573</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-9606
ispartof The Journal of chemical physics, 1998-02, Vol.108 (5), p.1932-1939
issn 0021-9606
1089-7690
language eng
recordid cdi_crossref_primary_10_1063_1_475573
source AIP Digital Archive
title The hindering of the inversion motion in the van der Waals aniline-Arn clusters: An adiabatic molecular dynamics simulation for n=1–3
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-11T15%3A53%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20hindering%20of%20the%20inversion%20motion%20in%20the%20van%20der%20Waals%20aniline-Arn%20clusters:%20An%20adiabatic%20molecular%20dynamics%20simulation%20for%20n=1%E2%80%933&rft.jtitle=The%20Journal%20of%20chemical%20physics&rft.au=Parneix,%20Pascal&rft.date=1998-02-01&rft.volume=108&rft.issue=5&rft.spage=1932&rft.epage=1939&rft.pages=1932-1939&rft.issn=0021-9606&rft.eissn=1089-7690&rft_id=info:doi/10.1063/1.475573&rft_dat=%3Ccrossref%3E10_1063_1_475573%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true