Revisiting electroaccepting and electrodonating powers: proposals for local electrophilicity and local nucleophilicity descriptors
The electrophilicity index, μ 2 /2 η , where μ is the chemical potential and η is the hardness, has been defined by Parr, Von Szentpaly, and Liu ( J. Am. Chem. Soc ., 1999, 121 , 1922) as the lowering in energy of an electronic system during a process in which the chemical potential of the system ra...
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creator | Morell, Christophe Gázquez, José L Vela, Alberto Guégan, Frédéric Chermette, Henry |
description | The electrophilicity index,
μ
2
/2
η
, where
μ
is the chemical potential and
η
is the hardness, has been defined by Parr, Von Szentpaly, and Liu (
J. Am. Chem. Soc
., 1999,
121
, 1922) as the lowering in energy of an electronic system during a process in which the chemical potential of the system raises from
μ
to zero, accepting −
μ
/
η
electrons. In this work, it is shown that the electrophilicity index is also a rational choice for measuring nucleophilicity. Indeed, within the grand canonical ensemble, when the chemical potential of a system increases from
μ
to zero, the system gives away
μ
/
η
electrons. During the process, the variation of the grand potential is
μ
2
/2
η
. Additionally, through the use of a second order Taylor series expansion of the density as a function of the number of electrons, at constant external potential, which depends on the Fukui function and the dual descriptor, the local electrophilicity is defined as the actual variation of the electron density when the system acquires −
μ
/
η
electrons, while the local nucleophilicity is similarly defined for the case when the system loses
μ
/
η
electrons.
It is shown that the electrophilicity index is also a rational choice for measuring nucleophilicity. |
doi_str_mv | 10.1039/c4cp03167a |
format | Article |
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μ
2
/2
η
, where
μ
is the chemical potential and
η
is the hardness, has been defined by Parr, Von Szentpaly, and Liu (
J. Am. Chem. Soc
., 1999,
121
, 1922) as the lowering in energy of an electronic system during a process in which the chemical potential of the system raises from
μ
to zero, accepting −
μ
/
η
electrons. In this work, it is shown that the electrophilicity index is also a rational choice for measuring nucleophilicity. Indeed, within the grand canonical ensemble, when the chemical potential of a system increases from
μ
to zero, the system gives away
μ
/
η
electrons. During the process, the variation of the grand potential is
μ
2
/2
η
. Additionally, through the use of a second order Taylor series expansion of the density as a function of the number of electrons, at constant external potential, which depends on the Fukui function and the dual descriptor, the local electrophilicity is defined as the actual variation of the electron density when the system acquires −
μ
/
η
electrons, while the local nucleophilicity is similarly defined for the case when the system loses
μ
/
η
electrons.
It is shown that the electrophilicity index is also a rational choice for measuring nucleophilicity.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/c4cp03167a</identifier><identifier>PMID: 25375814</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Analytical chemistry ; Chemical potential ; Chemical Sciences ; Constants ; Density ; Electron density ; Electronic systems ; Hardness ; Physical chemistry ; Taylor series</subject><ispartof>Physical chemistry chemical physics : PCCP, 2014-01, Vol.16 (48), p.26832-26842</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-f569d8612d4a3af34fb4e51f6bf7cb25bb80870901fba7c0883af9096bdd41b53</citedby><cites>FETCH-LOGICAL-c402t-f569d8612d4a3af34fb4e51f6bf7cb25bb80870901fba7c0883af9096bdd41b53</cites><orcidid>0000-0002-6321-8723 ; 0000-0002-5890-7479</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25375814$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01230136$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Morell, Christophe</creatorcontrib><creatorcontrib>Gázquez, José L</creatorcontrib><creatorcontrib>Vela, Alberto</creatorcontrib><creatorcontrib>Guégan, Frédéric</creatorcontrib><creatorcontrib>Chermette, Henry</creatorcontrib><title>Revisiting electroaccepting and electrodonating powers: proposals for local electrophilicity and local nucleophilicity descriptors</title><title>Physical chemistry chemical physics : PCCP</title><addtitle>Phys Chem Chem Phys</addtitle><description>The electrophilicity index,
μ
2
/2
η
, where
μ
is the chemical potential and
η
is the hardness, has been defined by Parr, Von Szentpaly, and Liu (
J. Am. Chem. Soc
., 1999,
121
, 1922) as the lowering in energy of an electronic system during a process in which the chemical potential of the system raises from
μ
to zero, accepting −
μ
/
η
electrons. In this work, it is shown that the electrophilicity index is also a rational choice for measuring nucleophilicity. Indeed, within the grand canonical ensemble, when the chemical potential of a system increases from
μ
to zero, the system gives away
μ
/
η
electrons. During the process, the variation of the grand potential is
μ
2
/2
η
. Additionally, through the use of a second order Taylor series expansion of the density as a function of the number of electrons, at constant external potential, which depends on the Fukui function and the dual descriptor, the local electrophilicity is defined as the actual variation of the electron density when the system acquires −
μ
/
η
electrons, while the local nucleophilicity is similarly defined for the case when the system loses
μ
/
η
electrons.
It is shown that the electrophilicity index is also a rational choice for measuring nucleophilicity.</description><subject>Analytical chemistry</subject><subject>Chemical potential</subject><subject>Chemical Sciences</subject><subject>Constants</subject><subject>Density</subject><subject>Electron density</subject><subject>Electronic systems</subject><subject>Hardness</subject><subject>Physical chemistry</subject><subject>Taylor series</subject><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqN0ktv1DAUBWALUdEHbNiDhl2pNHBv7DgJu9EIaKWRQAjWlp_UyBMbO1PULb-8adIZWCFWjs79dGXrhJDnCG8QaPdWM52AIm_kI3KCjNNlBy17fPhu-DE5LeUHAGCN9Ak5rmra1C2yE_L7i73xxQ--_76wweohR6m1TVMge7MPTezllKX4y-bybpFyTLHIUBYu5kWIWoa9Tdc-eO2H22nBPOp3Oti_JsYWnX0aYi5PyZEb99hnD-cZ-fbh_df15XLz6ePVerVZagbVsHQ170zLsTJMUukoc4rZGh1XrtGqqpVqoW2gA3RKNhradlQddFwZw1DV9Iy8nvdeyyBS9luZb0WUXlyuNuI-A6woIOU3ONrz2Y7P_LmzZRBbX7QNQfY27opAXiPDquv4f9CqGSuAiV7MVOdYSrbucA0EcV-lWLP156nK1YhfPuzdqa01B7rvbgSvZpCLPkz__AsiGTeaF_8y9A6eqbFY</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Morell, Christophe</creator><creator>Gázquez, José L</creator><creator>Vela, Alberto</creator><creator>Guégan, Frédéric</creator><creator>Chermette, Henry</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-6321-8723</orcidid><orcidid>https://orcid.org/0000-0002-5890-7479</orcidid></search><sort><creationdate>20140101</creationdate><title>Revisiting electroaccepting and electrodonating powers: proposals for local electrophilicity and local nucleophilicity descriptors</title><author>Morell, Christophe ; Gázquez, José L ; Vela, Alberto ; Guégan, Frédéric ; Chermette, Henry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-f569d8612d4a3af34fb4e51f6bf7cb25bb80870901fba7c0883af9096bdd41b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Analytical chemistry</topic><topic>Chemical potential</topic><topic>Chemical Sciences</topic><topic>Constants</topic><topic>Density</topic><topic>Electron density</topic><topic>Electronic systems</topic><topic>Hardness</topic><topic>Physical chemistry</topic><topic>Taylor series</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morell, Christophe</creatorcontrib><creatorcontrib>Gázquez, José L</creatorcontrib><creatorcontrib>Vela, Alberto</creatorcontrib><creatorcontrib>Guégan, Frédéric</creatorcontrib><creatorcontrib>Chermette, Henry</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morell, Christophe</au><au>Gázquez, José L</au><au>Vela, Alberto</au><au>Guégan, Frédéric</au><au>Chermette, Henry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Revisiting electroaccepting and electrodonating powers: proposals for local electrophilicity and local nucleophilicity descriptors</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><addtitle>Phys Chem Chem Phys</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>16</volume><issue>48</issue><spage>26832</spage><epage>26842</epage><pages>26832-26842</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>The electrophilicity index,
μ
2
/2
η
, where
μ
is the chemical potential and
η
is the hardness, has been defined by Parr, Von Szentpaly, and Liu (
J. Am. Chem. Soc
., 1999,
121
, 1922) as the lowering in energy of an electronic system during a process in which the chemical potential of the system raises from
μ
to zero, accepting −
μ
/
η
electrons. In this work, it is shown that the electrophilicity index is also a rational choice for measuring nucleophilicity. Indeed, within the grand canonical ensemble, when the chemical potential of a system increases from
μ
to zero, the system gives away
μ
/
η
electrons. During the process, the variation of the grand potential is
μ
2
/2
η
. Additionally, through the use of a second order Taylor series expansion of the density as a function of the number of electrons, at constant external potential, which depends on the Fukui function and the dual descriptor, the local electrophilicity is defined as the actual variation of the electron density when the system acquires −
μ
/
η
electrons, while the local nucleophilicity is similarly defined for the case when the system loses
μ
/
η
electrons.
It is shown that the electrophilicity index is also a rational choice for measuring nucleophilicity.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>25375814</pmid><doi>10.1039/c4cp03167a</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6321-8723</orcidid><orcidid>https://orcid.org/0000-0002-5890-7479</orcidid></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Analytical chemistry Chemical potential Chemical Sciences Constants Density Electron density Electronic systems Hardness Physical chemistry Taylor series |
title | Revisiting electroaccepting and electrodonating powers: proposals for local electrophilicity and local nucleophilicity descriptors |
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