Loading…
Molecular Recognition, Conformational Behavior, and Spectral Characteristics of Oxatub[4]arene Macrocycle
In the present work, we analyze molecular recognition behavior of synthetic hydroxylated oxatub[4]arene (TA4) receptor toward the methyl viologen in different redox states. The supramolecular binding of methyl viologen guest toward TA4 macrocyclic scaffold has been studied employing the dispersion...
Saved in:
Published in: | The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2018-01, Vol.122 (2), p.714-723 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a336t-4055368ad1e79236ca542e3ed5562a08c0f803ef07d7ec97503e23493bc8e1ad3 |
---|---|
cites | cdi_FETCH-LOGICAL-a336t-4055368ad1e79236ca542e3ed5562a08c0f803ef07d7ec97503e23493bc8e1ad3 |
container_end_page | 723 |
container_issue | 2 |
container_start_page | 714 |
container_title | The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory |
container_volume | 122 |
creator | Lande, Dipali N Gejji, Shridhar P |
description | In the present work, we analyze molecular recognition behavior of synthetic hydroxylated oxatub[4]arene (TA4) receptor toward the methyl viologen in different redox states. The supramolecular binding of methyl viologen guest toward TA4 macrocyclic scaffold has been studied employing the dispersion corrected ωB97X-D based density functional theory. The methyl viologen in dicationic and neutral forms revealed distinct features in electronic, 1H nuclear magnetic resonance, and infrared spectra. Quantum theory of atoms in molecules in conjunction with the noncovalent interaction reduced density gradient in real space have been used as tools to characterize the underlying host–guest binding. |
doi_str_mv | 10.1021/acs.jpca.7b12472 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1979966849</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1979966849</sourcerecordid><originalsourceid>FETCH-LOGICAL-a336t-4055368ad1e79236ca542e3ed5562a08c0f803ef07d7ec97503e23493bc8e1ad3</originalsourceid><addsrcrecordid>eNp1kEtPwzAQhC0EolC4c0I5cmiKH7ETH6HiJbWqxOOEULR1NjRVGhc7QfTf49LCjdPurGZGq4-QM0aHjHJ2CcYPFysDw3TGeJLyPXLEJKex5Ezuh51mOpZK6B459n5BKWWCJ4ekxzVXSsvsiFQTW6PpanDRIxr73lRtZZtBNLJNad0SNgrq6Brn8FlZN4igKaKnFZrWhfNoDg5Mi67ybWV8ZMto-gVtN3tN3sBhg9EEjLNmbWo8IQcl1B5Pd7NPXm5vnkf38Xh69zC6GscghGrjhEopVAYFw1RzoQzIhKPAQkrFgWaGlhkVWNK0SNHoVAbBRaLFzGTIoBB9crHtXTn70aFv82XlDdY1NGg7nzOdaq1UFiJ9QrfW8KP3Dst85aoluHXOaL4BnAfA-QZwvgMcIue79m62xOIv8Es0GAZbw0_Udi7g8__3fQOPF4gL</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1979966849</pqid></control><display><type>article</type><title>Molecular Recognition, Conformational Behavior, and Spectral Characteristics of Oxatub[4]arene Macrocycle</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Lande, Dipali N ; Gejji, Shridhar P</creator><creatorcontrib>Lande, Dipali N ; Gejji, Shridhar P</creatorcontrib><description>In the present work, we analyze molecular recognition behavior of synthetic hydroxylated oxatub[4]arene (TA4) receptor toward the methyl viologen in different redox states. The supramolecular binding of methyl viologen guest toward TA4 macrocyclic scaffold has been studied employing the dispersion corrected ωB97X-D based density functional theory. The methyl viologen in dicationic and neutral forms revealed distinct features in electronic, 1H nuclear magnetic resonance, and infrared spectra. Quantum theory of atoms in molecules in conjunction with the noncovalent interaction reduced density gradient in real space have been used as tools to characterize the underlying host–guest binding.</description><identifier>ISSN: 1089-5639</identifier><identifier>EISSN: 1520-5215</identifier><identifier>DOI: 10.1021/acs.jpca.7b12472</identifier><identifier>PMID: 29266958</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2018-01, Vol.122 (2), p.714-723</ispartof><rights>Copyright © 2017 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a336t-4055368ad1e79236ca542e3ed5562a08c0f803ef07d7ec97503e23493bc8e1ad3</citedby><cites>FETCH-LOGICAL-a336t-4055368ad1e79236ca542e3ed5562a08c0f803ef07d7ec97503e23493bc8e1ad3</cites><orcidid>0000-0003-3305-2475 ; 0000-0002-7219-1286</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29266958$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lande, Dipali N</creatorcontrib><creatorcontrib>Gejji, Shridhar P</creatorcontrib><title>Molecular Recognition, Conformational Behavior, and Spectral Characteristics of Oxatub[4]arene Macrocycle</title><title>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory</title><addtitle>J. Phys. Chem. A</addtitle><description>In the present work, we analyze molecular recognition behavior of synthetic hydroxylated oxatub[4]arene (TA4) receptor toward the methyl viologen in different redox states. The supramolecular binding of methyl viologen guest toward TA4 macrocyclic scaffold has been studied employing the dispersion corrected ωB97X-D based density functional theory. The methyl viologen in dicationic and neutral forms revealed distinct features in electronic, 1H nuclear magnetic resonance, and infrared spectra. Quantum theory of atoms in molecules in conjunction with the noncovalent interaction reduced density gradient in real space have been used as tools to characterize the underlying host–guest binding.</description><issn>1089-5639</issn><issn>1520-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kEtPwzAQhC0EolC4c0I5cmiKH7ETH6HiJbWqxOOEULR1NjRVGhc7QfTf49LCjdPurGZGq4-QM0aHjHJ2CcYPFysDw3TGeJLyPXLEJKex5Ezuh51mOpZK6B459n5BKWWCJ4ekxzVXSsvsiFQTW6PpanDRIxr73lRtZZtBNLJNad0SNgrq6Brn8FlZN4igKaKnFZrWhfNoDg5Mi67ybWV8ZMto-gVtN3tN3sBhg9EEjLNmbWo8IQcl1B5Pd7NPXm5vnkf38Xh69zC6GscghGrjhEopVAYFw1RzoQzIhKPAQkrFgWaGlhkVWNK0SNHoVAbBRaLFzGTIoBB9crHtXTn70aFv82XlDdY1NGg7nzOdaq1UFiJ9QrfW8KP3Dst85aoluHXOaL4BnAfA-QZwvgMcIue79m62xOIv8Es0GAZbw0_Udi7g8__3fQOPF4gL</recordid><startdate>20180118</startdate><enddate>20180118</enddate><creator>Lande, Dipali N</creator><creator>Gejji, Shridhar P</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3305-2475</orcidid><orcidid>https://orcid.org/0000-0002-7219-1286</orcidid></search><sort><creationdate>20180118</creationdate><title>Molecular Recognition, Conformational Behavior, and Spectral Characteristics of Oxatub[4]arene Macrocycle</title><author>Lande, Dipali N ; Gejji, Shridhar P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a336t-4055368ad1e79236ca542e3ed5562a08c0f803ef07d7ec97503e23493bc8e1ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lande, Dipali N</creatorcontrib><creatorcontrib>Gejji, Shridhar P</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lande, Dipali N</au><au>Gejji, Shridhar P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Recognition, Conformational Behavior, and Spectral Characteristics of Oxatub[4]arene Macrocycle</atitle><jtitle>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory</jtitle><addtitle>J. Phys. Chem. A</addtitle><date>2018-01-18</date><risdate>2018</risdate><volume>122</volume><issue>2</issue><spage>714</spage><epage>723</epage><pages>714-723</pages><issn>1089-5639</issn><eissn>1520-5215</eissn><abstract>In the present work, we analyze molecular recognition behavior of synthetic hydroxylated oxatub[4]arene (TA4) receptor toward the methyl viologen in different redox states. The supramolecular binding of methyl viologen guest toward TA4 macrocyclic scaffold has been studied employing the dispersion corrected ωB97X-D based density functional theory. The methyl viologen in dicationic and neutral forms revealed distinct features in electronic, 1H nuclear magnetic resonance, and infrared spectra. Quantum theory of atoms in molecules in conjunction with the noncovalent interaction reduced density gradient in real space have been used as tools to characterize the underlying host–guest binding.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>29266958</pmid><doi>10.1021/acs.jpca.7b12472</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-3305-2475</orcidid><orcidid>https://orcid.org/0000-0002-7219-1286</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1089-5639 |
ispartof | The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2018-01, Vol.122 (2), p.714-723 |
issn | 1089-5639 1520-5215 |
language | eng |
recordid | cdi_proquest_miscellaneous_1979966849 |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | Molecular Recognition, Conformational Behavior, and Spectral Characteristics of Oxatub[4]arene Macrocycle |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T10%3A30%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Molecular%20Recognition,%20Conformational%20Behavior,%20and%20Spectral%20Characteristics%20of%20Oxatub%5B4%5Darene%20Macrocycle&rft.jtitle=The%20journal%20of%20physical%20chemistry.%20A,%20Molecules,%20spectroscopy,%20kinetics,%20environment,%20&%20general%20theory&rft.au=Lande,%20Dipali%20N&rft.date=2018-01-18&rft.volume=122&rft.issue=2&rft.spage=714&rft.epage=723&rft.pages=714-723&rft.issn=1089-5639&rft.eissn=1520-5215&rft_id=info:doi/10.1021/acs.jpca.7b12472&rft_dat=%3Cproquest_cross%3E1979966849%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a336t-4055368ad1e79236ca542e3ed5562a08c0f803ef07d7ec97503e23493bc8e1ad3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1979966849&rft_id=info:pmid/29266958&rfr_iscdi=true |