Loading…
Steering Self‐Assembly of Three‐Dimensional Iptycenes on Au(111) by Tuning Molecule‐Surface Interactions
Self‐assembly of three‐dimensional molecules is scarcely studied on surfaces. Their modes of adsorption can exhibit far greater variability compared to (nearly) planar molecules that adsorb mostly flat on surfaces. This additional degree of freedom can have decisive consequences for the expression o...
Saved in:
Published in: | Angewandte Chemie International Edition 2022-06, Vol.61 (25), p.e202201044-n/a |
---|---|
Main Authors: | , , , , , , , , |
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-c5064-11eb2ab045ce8a77ee103795e2505cdbbd8c6933a0a4d79384d70669941c31ff3 |
---|---|
cites | cdi_FETCH-LOGICAL-c5064-11eb2ab045ce8a77ee103795e2505cdbbd8c6933a0a4d79384d70669941c31ff3 |
container_end_page | n/a |
container_issue | 25 |
container_start_page | e202201044 |
container_title | Angewandte Chemie International Edition |
container_volume | 61 |
creator | Grossmann, Lukas Ringel, Eva Rastgoo‐Lahrood, Atena King, Benjamin T. Rosen, Johanna Heckl, Wolfgang M. Opris, Dorina Björk, Jonas Lackinger, Markus |
description | Self‐assembly of three‐dimensional molecules is scarcely studied on surfaces. Their modes of adsorption can exhibit far greater variability compared to (nearly) planar molecules that adsorb mostly flat on surfaces. This additional degree of freedom can have decisive consequences for the expression of intermolecular binding motifs, hence the formation of supramolecular structures. The determining molecule‐surface interactions can be widely tuned, thereby providing a new powerful lever for crystal engineering in two dimensions. Here, we study the self‐assembly of triptycene derivatives with anthracene blades on Au(111) by Scanning Tunneling Microscopy, Near Edge X‐ray Absorption Fine Structure and Density Functional Theory. The impact of molecule‐surface interactions was experimentally tested by comparing pristine with iodine‐passivated Au(111) surfaces. Thereby, we observed a fundamental change of the adsorption mode that triggered self‐assembly of an entirely different structure.
Passivation of Au(111) with an iodine monolayer provides effective means to steer the adsorption of three‐dimensional (f)antrip molecules. The stronger interaction on pristine Au(111) favours adsorption with two anthracene blades flat, promoting self‐assembly of a densely packed structure. By contrast, on passivated Au(111) f(antrip) adsorbs with its three anthracene blades edge‐on, giving rise to self‐assembly of a porous structure. |
doi_str_mv | 10.1002/anie.202201044 |
format | article |
fullrecord | <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_DiVA_org_liu_184738</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2639229282</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5064-11eb2ab045ce8a77ee103795e2505cdbbd8c6933a0a4d79384d70669941c31ff3</originalsourceid><addsrcrecordid>eNqFkc1u1DAUhSMEoqWwZYkisSmLDP5JYnuDFLUFRiqwmIGt5Xhupq4ce7ATquz6CH1GngRHUwbKho1tXX_n6N57suwlRguMEHmrnIEFQYQgjMryUXaMK4ILyhh9nN4lpQXjFT7KnsV4nXjOUf00O6IV4YyU7DhzqwEgGLfNV2C7n7d3TYzQt3bKfZevrwJAqp2bHlw03imbL3fDpMFBzL3Lm_EUY_wmb6d8PbrZ5ZO3oEc7q1Zj6JSGfOkGCEoPSR-fZ086ZSO8uL9Psq_vL9ZnH4vLLx-WZ81loStUlwXG0BLVorLSwBVjABhRJiogFar0pm03XNeCUoVUuWGC8nSiuhaixJrirqMnWbH3jTewG1u5C6ZXYZJeGXluvjXSh620ZpSYl4zyxL_b8wnuYZMGHIKyD2QPf5y5klv_QwpKKlqzZHB6bxD89xHiIHsTNVirHPgxSlJTQYggnCT09T_otR9D2u1MsdROjUSVqMWe0sHHGKA7NIORnKOXc_TyEH0SvPp7hAP-O-sEiD1wYyxM_7GTzeflxR_zXycsvjQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2674736095</pqid></control><display><type>article</type><title>Steering Self‐Assembly of Three‐Dimensional Iptycenes on Au(111) by Tuning Molecule‐Surface Interactions</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Grossmann, Lukas ; Ringel, Eva ; Rastgoo‐Lahrood, Atena ; King, Benjamin T. ; Rosen, Johanna ; Heckl, Wolfgang M. ; Opris, Dorina ; Björk, Jonas ; Lackinger, Markus</creator><creatorcontrib>Grossmann, Lukas ; Ringel, Eva ; Rastgoo‐Lahrood, Atena ; King, Benjamin T. ; Rosen, Johanna ; Heckl, Wolfgang M. ; Opris, Dorina ; Björk, Jonas ; Lackinger, Markus</creatorcontrib><description>Self‐assembly of three‐dimensional molecules is scarcely studied on surfaces. Their modes of adsorption can exhibit far greater variability compared to (nearly) planar molecules that adsorb mostly flat on surfaces. This additional degree of freedom can have decisive consequences for the expression of intermolecular binding motifs, hence the formation of supramolecular structures. The determining molecule‐surface interactions can be widely tuned, thereby providing a new powerful lever for crystal engineering in two dimensions. Here, we study the self‐assembly of triptycene derivatives with anthracene blades on Au(111) by Scanning Tunneling Microscopy, Near Edge X‐ray Absorption Fine Structure and Density Functional Theory. The impact of molecule‐surface interactions was experimentally tested by comparing pristine with iodine‐passivated Au(111) surfaces. Thereby, we observed a fundamental change of the adsorption mode that triggered self‐assembly of an entirely different structure.
Passivation of Au(111) with an iodine monolayer provides effective means to steer the adsorption of three‐dimensional (f)antrip molecules. The stronger interaction on pristine Au(111) favours adsorption with two anthracene blades flat, promoting self‐assembly of a densely packed structure. By contrast, on passivated Au(111) f(antrip) adsorbs with its three anthracene blades edge‐on, giving rise to self‐assembly of a porous structure.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>ISSN: 1521-3773</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202201044</identifier><identifier>PMID: 35287247</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Adsorption ; Anthracene ; Assembly ; Crystal Engineering ; Density functional theory ; Fine structure ; Iodine ; Scanning Tunneling Microscopy ; Self-Assembly ; Steering ; Surface chemistry ; Surface-Passivation ; Triptycene ; Ultrastructure</subject><ispartof>Angewandte Chemie International Edition, 2022-06, Vol.61 (25), p.e202201044-n/a</ispartof><rights>2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH</rights><rights>2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.</rights><rights>2022. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5064-11eb2ab045ce8a77ee103795e2505cdbbd8c6933a0a4d79384d70669941c31ff3</citedby><cites>FETCH-LOGICAL-c5064-11eb2ab045ce8a77ee103795e2505cdbbd8c6933a0a4d79384d70669941c31ff3</cites><orcidid>0000-0002-0585-7500 ; 0000-0002-7384-9211 ; 0000-0002-1345-0006 ; 0000-0003-4226-4795</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35287247$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-184738$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Grossmann, Lukas</creatorcontrib><creatorcontrib>Ringel, Eva</creatorcontrib><creatorcontrib>Rastgoo‐Lahrood, Atena</creatorcontrib><creatorcontrib>King, Benjamin T.</creatorcontrib><creatorcontrib>Rosen, Johanna</creatorcontrib><creatorcontrib>Heckl, Wolfgang M.</creatorcontrib><creatorcontrib>Opris, Dorina</creatorcontrib><creatorcontrib>Björk, Jonas</creatorcontrib><creatorcontrib>Lackinger, Markus</creatorcontrib><title>Steering Self‐Assembly of Three‐Dimensional Iptycenes on Au(111) by Tuning Molecule‐Surface Interactions</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>Self‐assembly of three‐dimensional molecules is scarcely studied on surfaces. Their modes of adsorption can exhibit far greater variability compared to (nearly) planar molecules that adsorb mostly flat on surfaces. This additional degree of freedom can have decisive consequences for the expression of intermolecular binding motifs, hence the formation of supramolecular structures. The determining molecule‐surface interactions can be widely tuned, thereby providing a new powerful lever for crystal engineering in two dimensions. Here, we study the self‐assembly of triptycene derivatives with anthracene blades on Au(111) by Scanning Tunneling Microscopy, Near Edge X‐ray Absorption Fine Structure and Density Functional Theory. The impact of molecule‐surface interactions was experimentally tested by comparing pristine with iodine‐passivated Au(111) surfaces. Thereby, we observed a fundamental change of the adsorption mode that triggered self‐assembly of an entirely different structure.
Passivation of Au(111) with an iodine monolayer provides effective means to steer the adsorption of three‐dimensional (f)antrip molecules. The stronger interaction on pristine Au(111) favours adsorption with two anthracene blades flat, promoting self‐assembly of a densely packed structure. By contrast, on passivated Au(111) f(antrip) adsorbs with its three anthracene blades edge‐on, giving rise to self‐assembly of a porous structure.</description><subject>Adsorption</subject><subject>Anthracene</subject><subject>Assembly</subject><subject>Crystal Engineering</subject><subject>Density functional theory</subject><subject>Fine structure</subject><subject>Iodine</subject><subject>Scanning Tunneling Microscopy</subject><subject>Self-Assembly</subject><subject>Steering</subject><subject>Surface chemistry</subject><subject>Surface-Passivation</subject><subject>Triptycene</subject><subject>Ultrastructure</subject><issn>1433-7851</issn><issn>1521-3773</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkc1u1DAUhSMEoqWwZYkisSmLDP5JYnuDFLUFRiqwmIGt5Xhupq4ce7ATquz6CH1GngRHUwbKho1tXX_n6N57suwlRguMEHmrnIEFQYQgjMryUXaMK4ILyhh9nN4lpQXjFT7KnsV4nXjOUf00O6IV4YyU7DhzqwEgGLfNV2C7n7d3TYzQt3bKfZevrwJAqp2bHlw03imbL3fDpMFBzL3Lm_EUY_wmb6d8PbrZ5ZO3oEc7q1Zj6JSGfOkGCEoPSR-fZ086ZSO8uL9Psq_vL9ZnH4vLLx-WZ81loStUlwXG0BLVorLSwBVjABhRJiogFar0pm03XNeCUoVUuWGC8nSiuhaixJrirqMnWbH3jTewG1u5C6ZXYZJeGXluvjXSh620ZpSYl4zyxL_b8wnuYZMGHIKyD2QPf5y5klv_QwpKKlqzZHB6bxD89xHiIHsTNVirHPgxSlJTQYggnCT09T_otR9D2u1MsdROjUSVqMWe0sHHGKA7NIORnKOXc_TyEH0SvPp7hAP-O-sEiD1wYyxM_7GTzeflxR_zXycsvjQ</recordid><startdate>20220620</startdate><enddate>20220620</enddate><creator>Grossmann, Lukas</creator><creator>Ringel, Eva</creator><creator>Rastgoo‐Lahrood, Atena</creator><creator>King, Benjamin T.</creator><creator>Rosen, Johanna</creator><creator>Heckl, Wolfgang M.</creator><creator>Opris, Dorina</creator><creator>Björk, Jonas</creator><creator>Lackinger, Markus</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><scope>ABXSW</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DG8</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-0585-7500</orcidid><orcidid>https://orcid.org/0000-0002-7384-9211</orcidid><orcidid>https://orcid.org/0000-0002-1345-0006</orcidid><orcidid>https://orcid.org/0000-0003-4226-4795</orcidid></search><sort><creationdate>20220620</creationdate><title>Steering Self‐Assembly of Three‐Dimensional Iptycenes on Au(111) by Tuning Molecule‐Surface Interactions</title><author>Grossmann, Lukas ; Ringel, Eva ; Rastgoo‐Lahrood, Atena ; King, Benjamin T. ; Rosen, Johanna ; Heckl, Wolfgang M. ; Opris, Dorina ; Björk, Jonas ; Lackinger, Markus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5064-11eb2ab045ce8a77ee103795e2505cdbbd8c6933a0a4d79384d70669941c31ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adsorption</topic><topic>Anthracene</topic><topic>Assembly</topic><topic>Crystal Engineering</topic><topic>Density functional theory</topic><topic>Fine structure</topic><topic>Iodine</topic><topic>Scanning Tunneling Microscopy</topic><topic>Self-Assembly</topic><topic>Steering</topic><topic>Surface chemistry</topic><topic>Surface-Passivation</topic><topic>Triptycene</topic><topic>Ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grossmann, Lukas</creatorcontrib><creatorcontrib>Ringel, Eva</creatorcontrib><creatorcontrib>Rastgoo‐Lahrood, Atena</creatorcontrib><creatorcontrib>King, Benjamin T.</creatorcontrib><creatorcontrib>Rosen, Johanna</creatorcontrib><creatorcontrib>Heckl, Wolfgang M.</creatorcontrib><creatorcontrib>Opris, Dorina</creatorcontrib><creatorcontrib>Björk, Jonas</creatorcontrib><creatorcontrib>Lackinger, Markus</creatorcontrib><collection>Open Access: Wiley-Blackwell Open Access Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Linköpings universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Linköpings universitet</collection><collection>SwePub Articles full text</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grossmann, Lukas</au><au>Ringel, Eva</au><au>Rastgoo‐Lahrood, Atena</au><au>King, Benjamin T.</au><au>Rosen, Johanna</au><au>Heckl, Wolfgang M.</au><au>Opris, Dorina</au><au>Björk, Jonas</au><au>Lackinger, Markus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Steering Self‐Assembly of Three‐Dimensional Iptycenes on Au(111) by Tuning Molecule‐Surface Interactions</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2022-06-20</date><risdate>2022</risdate><volume>61</volume><issue>25</issue><spage>e202201044</spage><epage>n/a</epage><pages>e202201044-n/a</pages><issn>1433-7851</issn><issn>1521-3773</issn><eissn>1521-3773</eissn><abstract>Self‐assembly of three‐dimensional molecules is scarcely studied on surfaces. Their modes of adsorption can exhibit far greater variability compared to (nearly) planar molecules that adsorb mostly flat on surfaces. This additional degree of freedom can have decisive consequences for the expression of intermolecular binding motifs, hence the formation of supramolecular structures. The determining molecule‐surface interactions can be widely tuned, thereby providing a new powerful lever for crystal engineering in two dimensions. Here, we study the self‐assembly of triptycene derivatives with anthracene blades on Au(111) by Scanning Tunneling Microscopy, Near Edge X‐ray Absorption Fine Structure and Density Functional Theory. The impact of molecule‐surface interactions was experimentally tested by comparing pristine with iodine‐passivated Au(111) surfaces. Thereby, we observed a fundamental change of the adsorption mode that triggered self‐assembly of an entirely different structure.
Passivation of Au(111) with an iodine monolayer provides effective means to steer the adsorption of three‐dimensional (f)antrip molecules. The stronger interaction on pristine Au(111) favours adsorption with two anthracene blades flat, promoting self‐assembly of a densely packed structure. By contrast, on passivated Au(111) f(antrip) adsorbs with its three anthracene blades edge‐on, giving rise to self‐assembly of a porous structure.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35287247</pmid><doi>10.1002/anie.202201044</doi><tpages>6</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0002-0585-7500</orcidid><orcidid>https://orcid.org/0000-0002-7384-9211</orcidid><orcidid>https://orcid.org/0000-0002-1345-0006</orcidid><orcidid>https://orcid.org/0000-0003-4226-4795</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1433-7851 |
ispartof | Angewandte Chemie International Edition, 2022-06, Vol.61 (25), p.e202201044-n/a |
issn | 1433-7851 1521-3773 1521-3773 |
language | eng |
recordid | cdi_swepub_primary_oai_DiVA_org_liu_184738 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Adsorption Anthracene Assembly Crystal Engineering Density functional theory Fine structure Iodine Scanning Tunneling Microscopy Self-Assembly Steering Surface chemistry Surface-Passivation Triptycene Ultrastructure |
title | Steering Self‐Assembly of Three‐Dimensional Iptycenes on Au(111) by Tuning Molecule‐Surface Interactions |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T22%3A13%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Steering%20Self%E2%80%90Assembly%20of%20Three%E2%80%90Dimensional%20Iptycenes%20on%20Au(111)%20by%20Tuning%20Molecule%E2%80%90Surface%20Interactions&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Grossmann,%20Lukas&rft.date=2022-06-20&rft.volume=61&rft.issue=25&rft.spage=e202201044&rft.epage=n/a&rft.pages=e202201044-n/a&rft.issn=1433-7851&rft.eissn=1521-3773&rft_id=info:doi/10.1002/anie.202201044&rft_dat=%3Cproquest_swepu%3E2639229282%3C/proquest_swepu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5064-11eb2ab045ce8a77ee103795e2505cdbbd8c6933a0a4d79384d70669941c31ff3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2674736095&rft_id=info:pmid/35287247&rfr_iscdi=true |