A Pd3L6 supramolecular cage incorporating photoactive [2.2]paracyclophane units
[2.2]Paracyclophane (pCp) scaffolds, unlike many π-conjugated building blocks, have been rarely explored in supramolecular self-assembly. Herein we report the synthesis and characterization of two ligands, pCpd3py and pCpd4py, composed of a pCp core functionalized at its 7- and 15-positions respecti...
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creator | Diego Rota Martir Delforce, Lucie Cordes, David B Slawin, Alexandra M Z Warriner, Stuart L Jacquemin, Denis Zysman-Colman, Eli |
description | [2.2]Paracyclophane (pCp) scaffolds, unlike many π-conjugated building blocks, have been rarely explored in supramolecular self-assembly. Herein we report the synthesis and characterization of two ligands, pCpd3py and pCpd4py, composed of a pCp core functionalized at its 7- and 15-positions respectively with 3-pyridyl and 4-pyridyl units. The self-assembly of pCpd4py with Pd2+ metal ions afforded a [Pd3(pCpd4py)6]6+ cage structure, pCpd4py-Pd, where the six pCpd4py ligands doubly bridge each edge of the Pd3 triangular core. The ligand pCpd4py and the palladium cage pCpd4py-Pd have been characterized by NMR spectroscopy, ESI-MS spectrometry and X-ray diffraction analyses and their photophysical properties investigated by steady-state and time-resolved emission spectroscopy as well as time-dependent density functional theory calculations. |
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Herein we report the synthesis and characterization of two ligands, pCpd3py and pCpd4py, composed of a pCp core functionalized at its 7- and 15-positions respectively with 3-pyridyl and 4-pyridyl units. The self-assembly of pCpd4py with Pd2+ metal ions afforded a [Pd3(pCpd4py)6]6+ cage structure, pCpd4py-Pd, where the six pCpd4py ligands doubly bridge each edge of the Pd3 triangular core. The ligand pCpd4py and the palladium cage pCpd4py-Pd have been characterized by NMR spectroscopy, ESI-MS spectrometry and X-ray diffraction analyses and their photophysical properties investigated by steady-state and time-resolved emission spectroscopy as well as time-dependent density functional theory calculations.</description><identifier>ISSN: 2052-1545</identifier><identifier>EISSN: 2052-1553</identifier><identifier>DOI: 10.1039/c9qi01147a</identifier><language>eng</language><publisher>London: Royal Society of Chemistry</publisher><subject>Cages ; Crystal structure ; Crystallography ; Density functional theory ; Emission analysis ; Inorganic chemistry ; Ligands ; Mathematical analysis ; NMR spectroscopy ; Optoelectronics ; Palladium ; Self-assembly ; Time dependence</subject><ispartof>Inorganic chemistry frontiers, 2020-01, Vol.7 (1), p.232-238</ispartof><rights>Copyright Royal Society of Chemistry 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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></links><search><creatorcontrib>Diego Rota Martir</creatorcontrib><creatorcontrib>Delforce, Lucie</creatorcontrib><creatorcontrib>Cordes, David B</creatorcontrib><creatorcontrib>Slawin, Alexandra M Z</creatorcontrib><creatorcontrib>Warriner, Stuart L</creatorcontrib><creatorcontrib>Jacquemin, Denis</creatorcontrib><creatorcontrib>Zysman-Colman, Eli</creatorcontrib><title>A Pd3L6 supramolecular cage incorporating photoactive [2.2]paracyclophane units</title><title>Inorganic chemistry frontiers</title><description>[2.2]Paracyclophane (pCp) scaffolds, unlike many π-conjugated building blocks, have been rarely explored in supramolecular self-assembly. Herein we report the synthesis and characterization of two ligands, pCpd3py and pCpd4py, composed of a pCp core functionalized at its 7- and 15-positions respectively with 3-pyridyl and 4-pyridyl units. The self-assembly of pCpd4py with Pd2+ metal ions afforded a [Pd3(pCpd4py)6]6+ cage structure, pCpd4py-Pd, where the six pCpd4py ligands doubly bridge each edge of the Pd3 triangular core. The ligand pCpd4py and the palladium cage pCpd4py-Pd have been characterized by NMR spectroscopy, ESI-MS spectrometry and X-ray diffraction analyses and their photophysical properties investigated by steady-state and time-resolved emission spectroscopy as well as time-dependent density functional theory calculations.</description><subject>Cages</subject><subject>Crystal structure</subject><subject>Crystallography</subject><subject>Density functional theory</subject><subject>Emission analysis</subject><subject>Inorganic chemistry</subject><subject>Ligands</subject><subject>Mathematical analysis</subject><subject>NMR spectroscopy</subject><subject>Optoelectronics</subject><subject>Palladium</subject><subject>Self-assembly</subject><subject>Time dependence</subject><issn>2052-1545</issn><issn>2052-1553</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNo9jUtLAzEYRYMoWGo3_oKA66l5Z7IsxRcM1IWuRMo3mUwbGSdpkhH89w4oru7lHjgXoWtK1pRwc2vNyRNKhYYztGBEsopKyc__u5CXaJWzb8k8EEOJXqDdBj93vFE4TzHBZxicnQZI2MLBYT_akGJIUPx4wPEYSgBb_JfDb2zN3iMksN92CPEIo8PT6Eu-Qhc9DNmt_nKJXu_vXraPVbN7eNpumioyakrlVEuJqpWtAWQtFO87x63VsgPBOmFbR3ptSVcLwfoaDJ2B1qJ1WhutesOX6ObXG1M4TS6X_UeY0jhf7hlnmjNlZusPaP9RWA</recordid><startdate>20200107</startdate><enddate>20200107</enddate><creator>Diego Rota Martir</creator><creator>Delforce, Lucie</creator><creator>Cordes, David B</creator><creator>Slawin, Alexandra M Z</creator><creator>Warriner, Stuart L</creator><creator>Jacquemin, Denis</creator><creator>Zysman-Colman, Eli</creator><general>Royal Society of Chemistry</general><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20200107</creationdate><title>A Pd3L6 supramolecular cage incorporating photoactive [2.2]paracyclophane units</title><author>Diego Rota Martir ; Delforce, Lucie ; Cordes, David B ; Slawin, Alexandra M Z ; Warriner, Stuart L ; Jacquemin, Denis ; Zysman-Colman, Eli</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p219t-e6b10686c8aa58463fde3cc75da42d4cbe0f7c0d8442f8a915da774be77976f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cages</topic><topic>Crystal structure</topic><topic>Crystallography</topic><topic>Density functional theory</topic><topic>Emission analysis</topic><topic>Inorganic chemistry</topic><topic>Ligands</topic><topic>Mathematical analysis</topic><topic>NMR spectroscopy</topic><topic>Optoelectronics</topic><topic>Palladium</topic><topic>Self-assembly</topic><topic>Time dependence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Diego Rota Martir</creatorcontrib><creatorcontrib>Delforce, Lucie</creatorcontrib><creatorcontrib>Cordes, David B</creatorcontrib><creatorcontrib>Slawin, Alexandra M Z</creatorcontrib><creatorcontrib>Warriner, Stuart L</creatorcontrib><creatorcontrib>Jacquemin, Denis</creatorcontrib><creatorcontrib>Zysman-Colman, Eli</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Inorganic chemistry frontiers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Diego Rota Martir</au><au>Delforce, Lucie</au><au>Cordes, David B</au><au>Slawin, Alexandra M Z</au><au>Warriner, Stuart L</au><au>Jacquemin, Denis</au><au>Zysman-Colman, Eli</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Pd3L6 supramolecular cage incorporating photoactive [2.2]paracyclophane units</atitle><jtitle>Inorganic chemistry frontiers</jtitle><date>2020-01-07</date><risdate>2020</risdate><volume>7</volume><issue>1</issue><spage>232</spage><epage>238</epage><pages>232-238</pages><issn>2052-1545</issn><eissn>2052-1553</eissn><abstract>[2.2]Paracyclophane (pCp) scaffolds, unlike many π-conjugated building blocks, have been rarely explored in supramolecular self-assembly. Herein we report the synthesis and characterization of two ligands, pCpd3py and pCpd4py, composed of a pCp core functionalized at its 7- and 15-positions respectively with 3-pyridyl and 4-pyridyl units. The self-assembly of pCpd4py with Pd2+ metal ions afforded a [Pd3(pCpd4py)6]6+ cage structure, pCpd4py-Pd, where the six pCpd4py ligands doubly bridge each edge of the Pd3 triangular core. The ligand pCpd4py and the palladium cage pCpd4py-Pd have been characterized by NMR spectroscopy, ESI-MS spectrometry and X-ray diffraction analyses and their photophysical properties investigated by steady-state and time-resolved emission spectroscopy as well as time-dependent density functional theory calculations.</abstract><cop>London</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c9qi01147a</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cages Crystal structure Crystallography Density functional theory Emission analysis Inorganic chemistry Ligands Mathematical analysis NMR spectroscopy Optoelectronics Palladium Self-assembly Time dependence |
title | A Pd3L6 supramolecular cage incorporating photoactive [2.2]paracyclophane units |
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