Loading…

The Chameleonic Nature of Diazaperopyrenium Recognition Processes

Two for the price of one! The diazaperopyrenium dication behaves dichotomously in a homo‐ and heterophilic manner, allowing for complexation with itself and a variety of π‐electron‐rich donors. This chameleonic characteristic, in addition to its electronic properties, leads to self‐assembled nanowir...

Full description

Saved in:
Bibliographic Details
Published in:Angewandte Chemie International Edition 2012-11, Vol.51 (47), p.11872-11877
Main Authors: Basuray, Ashish N., Jacquot de Rouville, Henri-Pierre, Hartlieb, Karel J., Kikuchi, Takashi, Strutt, Nathan L., Bruns, Carson J., Ambrogio, Michael W., Avestro, Alyssa-Jennifer, Schneebeli, Severin T., Fahrenbach, Albert C., Stoddart, J. Fraser
Format: Article
Language:English
Subjects:
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-c4449-70128ed5f92a26aa1942d56e80dab3ba679785e6ec4d114be2d7cf1b298dea183
cites cdi_FETCH-LOGICAL-c4449-70128ed5f92a26aa1942d56e80dab3ba679785e6ec4d114be2d7cf1b298dea183
container_end_page 11877
container_issue 47
container_start_page 11872
container_title Angewandte Chemie International Edition
container_volume 51
creator Basuray, Ashish N.
Jacquot de Rouville, Henri-Pierre
Hartlieb, Karel J.
Kikuchi, Takashi
Strutt, Nathan L.
Bruns, Carson J.
Ambrogio, Michael W.
Avestro, Alyssa-Jennifer
Schneebeli, Severin T.
Fahrenbach, Albert C.
Stoddart, J. Fraser
description Two for the price of one! The diazaperopyrenium dication behaves dichotomously in a homo‐ and heterophilic manner, allowing for complexation with itself and a variety of π‐electron‐rich donors. This chameleonic characteristic, in addition to its electronic properties, leads to self‐assembled nanowires in the solid state, as well as to its acting as a template for aromatic crown ethers to form a [3]‐ and two [2]rotaxanes (see picture).
doi_str_mv 10.1002/anie.201205089
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1701036729</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1171848858</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4449-70128ed5f92a26aa1942d56e80dab3ba679785e6ec4d114be2d7cf1b298dea183</originalsourceid><addsrcrecordid>eNqFkc9v0zAYhi0EYmNw5YgiceGSzp8d_zpWZYyJqpvQEBIXy0m-MI8k7uxGUP56XHWr0C472Yfnffx9fgl5C3QGlLJTN3qcMQqMCqrNM3IMgkHJleLP873ivFRawBF5ldJt5rWm8iU5Ypwybow4JvPrGywWN27AHsPom2LlNlPEInTFR-_-ujXGsN5GHP00FF-xCT9Hv_FhLK5iaDAlTK_Ji871Cd_cnyfk26ez68Xncnl5frGYL8umqipTqjyjxlZ0hjkmnQNTsVZI1LR1Na-dVCZPihKbqgWoamStajqomdEtOtD8hHzYe9cx3E2YNnbwqcG-dyOGKVnIL1AuFTNPo6BAV1qLnfX9I_Q2THHMi2RKgDRUAsvUbE81MaQUsbPr6AcXtxao3fVgdz3YQw858O5eO9UDtgf84eMzYPbAb9_j9gmdna8uzv6Xl_usTxv8c8i6-MtKxZWw31fn9gcTX9TSXNkV_wcHqaIB</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1151690612</pqid></control><display><type>article</type><title>The Chameleonic Nature of Diazaperopyrenium Recognition Processes</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Basuray, Ashish N. ; Jacquot de Rouville, Henri-Pierre ; Hartlieb, Karel J. ; Kikuchi, Takashi ; Strutt, Nathan L. ; Bruns, Carson J. ; Ambrogio, Michael W. ; Avestro, Alyssa-Jennifer ; Schneebeli, Severin T. ; Fahrenbach, Albert C. ; Stoddart, J. Fraser</creator><creatorcontrib>Basuray, Ashish N. ; Jacquot de Rouville, Henri-Pierre ; Hartlieb, Karel J. ; Kikuchi, Takashi ; Strutt, Nathan L. ; Bruns, Carson J. ; Ambrogio, Michael W. ; Avestro, Alyssa-Jennifer ; Schneebeli, Severin T. ; Fahrenbach, Albert C. ; Stoddart, J. Fraser</creatorcontrib><description>Two for the price of one! The diazaperopyrenium dication behaves dichotomously in a homo‐ and heterophilic manner, allowing for complexation with itself and a variety of π‐electron‐rich donors. This chameleonic characteristic, in addition to its electronic properties, leads to self‐assembled nanowires in the solid state, as well as to its acting as a template for aromatic crown ethers to form a [3]‐ and two [2]rotaxanes (see picture).</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201205089</identifier><identifier>PMID: 23023995</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Complexation ; Crown ethers ; Donors (electronic) ; Electronic properties ; Nanowires ; noncovalent interactions ; perylene ; Pictures ; Recognition ; rotaxanes ; self-assembly ; Solid state ; supramolecular chemistry</subject><ispartof>Angewandte Chemie International Edition, 2012-11, Vol.51 (47), p.11872-11877</ispartof><rights>Copyright © 2012 WILEY‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>Copyright © 2012 WILEY-VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4449-70128ed5f92a26aa1942d56e80dab3ba679785e6ec4d114be2d7cf1b298dea183</citedby><cites>FETCH-LOGICAL-c4449-70128ed5f92a26aa1942d56e80dab3ba679785e6ec4d114be2d7cf1b298dea183</cites></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/23023995$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Basuray, Ashish N.</creatorcontrib><creatorcontrib>Jacquot de Rouville, Henri-Pierre</creatorcontrib><creatorcontrib>Hartlieb, Karel J.</creatorcontrib><creatorcontrib>Kikuchi, Takashi</creatorcontrib><creatorcontrib>Strutt, Nathan L.</creatorcontrib><creatorcontrib>Bruns, Carson J.</creatorcontrib><creatorcontrib>Ambrogio, Michael W.</creatorcontrib><creatorcontrib>Avestro, Alyssa-Jennifer</creatorcontrib><creatorcontrib>Schneebeli, Severin T.</creatorcontrib><creatorcontrib>Fahrenbach, Albert C.</creatorcontrib><creatorcontrib>Stoddart, J. Fraser</creatorcontrib><title>The Chameleonic Nature of Diazaperopyrenium Recognition Processes</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. Chem. Int. Ed</addtitle><description>Two for the price of one! The diazaperopyrenium dication behaves dichotomously in a homo‐ and heterophilic manner, allowing for complexation with itself and a variety of π‐electron‐rich donors. This chameleonic characteristic, in addition to its electronic properties, leads to self‐assembled nanowires in the solid state, as well as to its acting as a template for aromatic crown ethers to form a [3]‐ and two [2]rotaxanes (see picture).</description><subject>Complexation</subject><subject>Crown ethers</subject><subject>Donors (electronic)</subject><subject>Electronic properties</subject><subject>Nanowires</subject><subject>noncovalent interactions</subject><subject>perylene</subject><subject>Pictures</subject><subject>Recognition</subject><subject>rotaxanes</subject><subject>self-assembly</subject><subject>Solid state</subject><subject>supramolecular chemistry</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkc9v0zAYhi0EYmNw5YgiceGSzp8d_zpWZYyJqpvQEBIXy0m-MI8k7uxGUP56XHWr0C472Yfnffx9fgl5C3QGlLJTN3qcMQqMCqrNM3IMgkHJleLP873ivFRawBF5ldJt5rWm8iU5Ypwybow4JvPrGywWN27AHsPom2LlNlPEInTFR-_-ujXGsN5GHP00FF-xCT9Hv_FhLK5iaDAlTK_Ji871Cd_cnyfk26ez68Xncnl5frGYL8umqipTqjyjxlZ0hjkmnQNTsVZI1LR1Na-dVCZPihKbqgWoamStajqomdEtOtD8hHzYe9cx3E2YNnbwqcG-dyOGKVnIL1AuFTNPo6BAV1qLnfX9I_Q2THHMi2RKgDRUAsvUbE81MaQUsbPr6AcXtxao3fVgdz3YQw858O5eO9UDtgf84eMzYPbAb9_j9gmdna8uzv6Xl_usTxv8c8i6-MtKxZWw31fn9gcTX9TSXNkV_wcHqaIB</recordid><startdate>20121119</startdate><enddate>20121119</enddate><creator>Basuray, Ashish N.</creator><creator>Jacquot de Rouville, Henri-Pierre</creator><creator>Hartlieb, Karel J.</creator><creator>Kikuchi, Takashi</creator><creator>Strutt, Nathan L.</creator><creator>Bruns, Carson J.</creator><creator>Ambrogio, Michael W.</creator><creator>Avestro, Alyssa-Jennifer</creator><creator>Schneebeli, Severin T.</creator><creator>Fahrenbach, Albert C.</creator><creator>Stoddart, J. Fraser</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20121119</creationdate><title>The Chameleonic Nature of Diazaperopyrenium Recognition Processes</title><author>Basuray, Ashish N. ; Jacquot de Rouville, Henri-Pierre ; Hartlieb, Karel J. ; Kikuchi, Takashi ; Strutt, Nathan L. ; Bruns, Carson J. ; Ambrogio, Michael W. ; Avestro, Alyssa-Jennifer ; Schneebeli, Severin T. ; Fahrenbach, Albert C. ; Stoddart, J. Fraser</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4449-70128ed5f92a26aa1942d56e80dab3ba679785e6ec4d114be2d7cf1b298dea183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Complexation</topic><topic>Crown ethers</topic><topic>Donors (electronic)</topic><topic>Electronic properties</topic><topic>Nanowires</topic><topic>noncovalent interactions</topic><topic>perylene</topic><topic>Pictures</topic><topic>Recognition</topic><topic>rotaxanes</topic><topic>self-assembly</topic><topic>Solid state</topic><topic>supramolecular chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Basuray, Ashish N.</creatorcontrib><creatorcontrib>Jacquot de Rouville, Henri-Pierre</creatorcontrib><creatorcontrib>Hartlieb, Karel J.</creatorcontrib><creatorcontrib>Kikuchi, Takashi</creatorcontrib><creatorcontrib>Strutt, Nathan L.</creatorcontrib><creatorcontrib>Bruns, Carson J.</creatorcontrib><creatorcontrib>Ambrogio, Michael W.</creatorcontrib><creatorcontrib>Avestro, Alyssa-Jennifer</creatorcontrib><creatorcontrib>Schneebeli, Severin T.</creatorcontrib><creatorcontrib>Fahrenbach, Albert C.</creatorcontrib><creatorcontrib>Stoddart, J. Fraser</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Basuray, Ashish N.</au><au>Jacquot de Rouville, Henri-Pierre</au><au>Hartlieb, Karel J.</au><au>Kikuchi, Takashi</au><au>Strutt, Nathan L.</au><au>Bruns, Carson J.</au><au>Ambrogio, Michael W.</au><au>Avestro, Alyssa-Jennifer</au><au>Schneebeli, Severin T.</au><au>Fahrenbach, Albert C.</au><au>Stoddart, J. Fraser</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Chameleonic Nature of Diazaperopyrenium Recognition Processes</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew. Chem. Int. Ed</addtitle><date>2012-11-19</date><risdate>2012</risdate><volume>51</volume><issue>47</issue><spage>11872</spage><epage>11877</epage><pages>11872-11877</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>Two for the price of one! The diazaperopyrenium dication behaves dichotomously in a homo‐ and heterophilic manner, allowing for complexation with itself and a variety of π‐electron‐rich donors. This chameleonic characteristic, in addition to its electronic properties, leads to self‐assembled nanowires in the solid state, as well as to its acting as a template for aromatic crown ethers to form a [3]‐ and two [2]rotaxanes (see picture).</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>23023995</pmid><doi>10.1002/anie.201205089</doi><tpages>6</tpages><edition>International ed. in English</edition></addata></record>
fulltext fulltext
identifier ISSN: 1433-7851
ispartof Angewandte Chemie International Edition, 2012-11, Vol.51 (47), p.11872-11877
issn 1433-7851
1521-3773
language eng
recordid cdi_proquest_miscellaneous_1701036729
source Wiley-Blackwell Read & Publish Collection
subjects Complexation
Crown ethers
Donors (electronic)
Electronic properties
Nanowires
noncovalent interactions
perylene
Pictures
Recognition
rotaxanes
self-assembly
Solid state
supramolecular chemistry
title The Chameleonic Nature of Diazaperopyrenium Recognition Processes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T12%3A23%3A49IST&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=The%20Chameleonic%20Nature%20of%20Diazaperopyrenium%20Recognition%20Processes&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Basuray,%20Ashish%20N.&rft.date=2012-11-19&rft.volume=51&rft.issue=47&rft.spage=11872&rft.epage=11877&rft.pages=11872-11877&rft.issn=1433-7851&rft.eissn=1521-3773&rft.coden=ACIEAY&rft_id=info:doi/10.1002/anie.201205089&rft_dat=%3Cproquest_cross%3E1171848858%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4449-70128ed5f92a26aa1942d56e80dab3ba679785e6ec4d114be2d7cf1b298dea183%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1151690612&rft_id=info:pmid/23023995&rfr_iscdi=true