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Structures and Luminescent Sensing Properties of Terbium Metal–Organic Frameworks with Methyl-Decorated Phenanthroline Ligand
Two new Tb(III) metal–organic frameworks based on 4,7-dimethylphenanthroline (dmphen) and flexible ligand trans-1,4-cyclohexanedicarboxylate (chdc2−) were synthesized and characterized. Their crystallographic formulae are [Tb2(dmphen)2(H2O)2(chdc)3]·2DMF (1; DMF = N,N-dimethylformamide) and [Tb2(dmp...
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Published in: | Crystals (Basel) 2024-12, Vol.14 (12), p.1026 |
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description | Two new Tb(III) metal–organic frameworks based on 4,7-dimethylphenanthroline (dmphen) and flexible ligand trans-1,4-cyclohexanedicarboxylate (chdc2−) were synthesized and characterized. Their crystallographic formulae are [Tb2(dmphen)2(H2O)2(chdc)3]·2DMF (1; DMF = N,N-dimethylformamide) and [Tb2(dmphen)2(NO3)2(chdc)2]·2DMF (2). Among some differences in their synthetic conditions, the most important one is apparently the using of terbium(III) nitrate instead of terbium(III) chloride as a metal precursor in the synthesis of 2, providing a nitrate coordination to Tb3+, and its subsequent notable structural differences to 1. Compound 1 was found to have a layered hcb structure with intralayer windows ca. 10 × 8 Å2 in size. Its layer-to-layer packing leaves narrow channels running across these windows, with 18% as a total solvent-accessible volume in the coordination structure. Compound 2 was found to have a layered sql structure with smaller intralayer windows of ca. 8 × 6 Å2 in size. Methyl substituents on the phen ligands do not affect the topology of the framework but seem to have a substantial effect on the packing density, as well as the pore volume of the resulting MOF. A high 18.4% luminescence quantum yield was found for 2. Its emission lifetime of 0.695(12) ms belongs to a typical range for phosphorescent Tb(III)-carboxylate complexes. A quenching of its emission by different nitroaromatic molecules was found. A linear concentration dependence on 3-nitrotoluene and 4-nitro-m-xylene at micromolar concentrations was found during luminescent titration experiments (LOD values ca. 350 nM), suggesting this MOF to be a viable and highly sensitive luminescent sensor for such substrates. |
doi_str_mv | 10.3390/cryst14121026 |
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Their crystallographic formulae are [Tb2(dmphen)2(H2O)2(chdc)3]·2DMF (1; DMF = N,N-dimethylformamide) and [Tb2(dmphen)2(NO3)2(chdc)2]·2DMF (2). Among some differences in their synthetic conditions, the most important one is apparently the using of terbium(III) nitrate instead of terbium(III) chloride as a metal precursor in the synthesis of 2, providing a nitrate coordination to Tb3+, and its subsequent notable structural differences to 1. Compound 1 was found to have a layered hcb structure with intralayer windows ca. 10 × 8 Å2 in size. Its layer-to-layer packing leaves narrow channels running across these windows, with 18% as a total solvent-accessible volume in the coordination structure. Compound 2 was found to have a layered sql structure with smaller intralayer windows of ca. 8 × 6 Å2 in size. Methyl substituents on the phen ligands do not affect the topology of the framework but seem to have a substantial effect on the packing density, as well as the pore volume of the resulting MOF. A high 18.4% luminescence quantum yield was found for 2. Its emission lifetime of 0.695(12) ms belongs to a typical range for phosphorescent Tb(III)-carboxylate complexes. A quenching of its emission by different nitroaromatic molecules was found. A linear concentration dependence on 3-nitrotoluene and 4-nitro-m-xylene at micromolar concentrations was found during luminescent titration experiments (LOD values ca. 350 nM), suggesting this MOF to be a viable and highly sensitive luminescent sensor for such substrates.</description><identifier>ISSN: 2073-4352</identifier><identifier>EISSN: 2073-4352</identifier><identifier>DOI: 10.3390/cryst14121026</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Acids ; Analysis ; Coordination ; coordination polymers ; Crystallography ; Dimethylformamide ; Emission ; Ligands ; luminescence ; Metal-organic frameworks ; nitroaromatic ; Nitrotoluene ; Packing density ; Phosphorescence ; sensing ; Substrates ; Terbium ; terbium(III) ; Titration ; Topology ; Xylene</subject><ispartof>Crystals (Basel), 2024-12, Vol.14 (12), p.1026</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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><cites>FETCH-LOGICAL-c2106-71f2e9a5311eef0a6dcf634ad7e6637d6e9145fc33c8f6990f1871b6572eb19e3</cites><orcidid>0000-0001-8779-0612 ; 0000-0001-5272-8878 ; 0000-0001-8922-0066</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3149569855/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3149569855?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25752,27923,27924,37011,44589,74997</link.rule.ids></links><search><creatorcontrib>Ovchinnikova, Anna A.</creatorcontrib><creatorcontrib>Demakov, Pavel A.</creatorcontrib><creatorcontrib>Ryadun, Alexey A.</creatorcontrib><creatorcontrib>Fedin, Vladimir P.</creatorcontrib><creatorcontrib>Dybtsev, Danil N.</creatorcontrib><title>Structures and Luminescent Sensing Properties of Terbium Metal–Organic Frameworks with Methyl-Decorated Phenanthroline Ligand</title><title>Crystals (Basel)</title><description>Two new Tb(III) metal–organic frameworks based on 4,7-dimethylphenanthroline (dmphen) and flexible ligand trans-1,4-cyclohexanedicarboxylate (chdc2−) were synthesized and characterized. Their crystallographic formulae are [Tb2(dmphen)2(H2O)2(chdc)3]·2DMF (1; DMF = N,N-dimethylformamide) and [Tb2(dmphen)2(NO3)2(chdc)2]·2DMF (2). Among some differences in their synthetic conditions, the most important one is apparently the using of terbium(III) nitrate instead of terbium(III) chloride as a metal precursor in the synthesis of 2, providing a nitrate coordination to Tb3+, and its subsequent notable structural differences to 1. Compound 1 was found to have a layered hcb structure with intralayer windows ca. 10 × 8 Å2 in size. Its layer-to-layer packing leaves narrow channels running across these windows, with 18% as a total solvent-accessible volume in the coordination structure. Compound 2 was found to have a layered sql structure with smaller intralayer windows of ca. 8 × 6 Å2 in size. Methyl substituents on the phen ligands do not affect the topology of the framework but seem to have a substantial effect on the packing density, as well as the pore volume of the resulting MOF. A high 18.4% luminescence quantum yield was found for 2. Its emission lifetime of 0.695(12) ms belongs to a typical range for phosphorescent Tb(III)-carboxylate complexes. A quenching of its emission by different nitroaromatic molecules was found. A linear concentration dependence on 3-nitrotoluene and 4-nitro-m-xylene at micromolar concentrations was found during luminescent titration experiments (LOD values ca. 350 nM), suggesting this MOF to be a viable and highly sensitive luminescent sensor for such substrates.</description><subject>Acids</subject><subject>Analysis</subject><subject>Coordination</subject><subject>coordination polymers</subject><subject>Crystallography</subject><subject>Dimethylformamide</subject><subject>Emission</subject><subject>Ligands</subject><subject>luminescence</subject><subject>Metal-organic frameworks</subject><subject>nitroaromatic</subject><subject>Nitrotoluene</subject><subject>Packing density</subject><subject>Phosphorescence</subject><subject>sensing</subject><subject>Substrates</subject><subject>Terbium</subject><subject>terbium(III)</subject><subject>Titration</subject><subject>Topology</subject><subject>Xylene</subject><issn>2073-4352</issn><issn>2073-4352</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpVUcFOHDEMHVVFKgKOvUfqeWgymSSTI6KlRVoEEvQ8ymSc3Wxnkq2TEdpT-Qf-sF_S0K2qYh9s2e8923JVvWf0nHNNP1rcp8xa1jDayDfVcUMVr1sumrf_5e-qs5S2tJiSVCl2XP28z7jYvCAkYsJIVsvsAyQLIZN7CMmHNbnDuAPMvkCiIw-Ag19mcgPZTL-enm9xbYK35ArNDI8Rvyfy6PPmpb_ZT_UnsBFNhpHcbSCYkDcYpzKCrHzhjafVkTNTgrO_8aT6dvX54fJrvbr9cn15saptOUjWirkGtBGcMQBHjRytk7w1owIpuRolaNYKZzm3nZNaU8c6xQYpVAMD08BPquuD7hjNtt-hnw3u-2h8_6cQcd2bcqKdoOdDo8pMPeqOt0ILo6DrWgBBB8sEY0Xrw0Frh_HHAin327hgKOv3nLVaSN0JUVDnB9TaFFEfXMxobPERZm9jAOdL_aJrmJKNbnUh1AeCxZgSgvu3JqP9y4_7Vz_mvwGqnpvo</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Ovchinnikova, Anna A.</creator><creator>Demakov, Pavel A.</creator><creator>Ryadun, Alexey A.</creator><creator>Fedin, Vladimir P.</creator><creator>Dybtsev, Danil N.</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8779-0612</orcidid><orcidid>https://orcid.org/0000-0001-5272-8878</orcidid><orcidid>https://orcid.org/0000-0001-8922-0066</orcidid></search><sort><creationdate>20241201</creationdate><title>Structures and Luminescent Sensing Properties of Terbium Metal–Organic Frameworks with Methyl-Decorated Phenanthroline Ligand</title><author>Ovchinnikova, Anna A. ; Demakov, Pavel A. ; Ryadun, Alexey A. ; Fedin, Vladimir P. ; Dybtsev, Danil N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2106-71f2e9a5311eef0a6dcf634ad7e6637d6e9145fc33c8f6990f1871b6572eb19e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acids</topic><topic>Analysis</topic><topic>Coordination</topic><topic>coordination polymers</topic><topic>Crystallography</topic><topic>Dimethylformamide</topic><topic>Emission</topic><topic>Ligands</topic><topic>luminescence</topic><topic>Metal-organic frameworks</topic><topic>nitroaromatic</topic><topic>Nitrotoluene</topic><topic>Packing density</topic><topic>Phosphorescence</topic><topic>sensing</topic><topic>Substrates</topic><topic>Terbium</topic><topic>terbium(III)</topic><topic>Titration</topic><topic>Topology</topic><topic>Xylene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ovchinnikova, Anna A.</creatorcontrib><creatorcontrib>Demakov, Pavel A.</creatorcontrib><creatorcontrib>Ryadun, Alexey A.</creatorcontrib><creatorcontrib>Fedin, Vladimir P.</creatorcontrib><creatorcontrib>Dybtsev, Danil N.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Directory of Open Access Journals (Open Access)</collection><jtitle>Crystals (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ovchinnikova, Anna A.</au><au>Demakov, Pavel A.</au><au>Ryadun, Alexey A.</au><au>Fedin, Vladimir P.</au><au>Dybtsev, Danil N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structures and Luminescent Sensing Properties of Terbium Metal–Organic Frameworks with Methyl-Decorated Phenanthroline Ligand</atitle><jtitle>Crystals (Basel)</jtitle><date>2024-12-01</date><risdate>2024</risdate><volume>14</volume><issue>12</issue><spage>1026</spage><pages>1026-</pages><issn>2073-4352</issn><eissn>2073-4352</eissn><abstract>Two new Tb(III) metal–organic frameworks based on 4,7-dimethylphenanthroline (dmphen) and flexible ligand trans-1,4-cyclohexanedicarboxylate (chdc2−) were synthesized and characterized. Their crystallographic formulae are [Tb2(dmphen)2(H2O)2(chdc)3]·2DMF (1; DMF = N,N-dimethylformamide) and [Tb2(dmphen)2(NO3)2(chdc)2]·2DMF (2). Among some differences in their synthetic conditions, the most important one is apparently the using of terbium(III) nitrate instead of terbium(III) chloride as a metal precursor in the synthesis of 2, providing a nitrate coordination to Tb3+, and its subsequent notable structural differences to 1. Compound 1 was found to have a layered hcb structure with intralayer windows ca. 10 × 8 Å2 in size. Its layer-to-layer packing leaves narrow channels running across these windows, with 18% as a total solvent-accessible volume in the coordination structure. Compound 2 was found to have a layered sql structure with smaller intralayer windows of ca. 8 × 6 Å2 in size. Methyl substituents on the phen ligands do not affect the topology of the framework but seem to have a substantial effect on the packing density, as well as the pore volume of the resulting MOF. A high 18.4% luminescence quantum yield was found for 2. Its emission lifetime of 0.695(12) ms belongs to a typical range for phosphorescent Tb(III)-carboxylate complexes. A quenching of its emission by different nitroaromatic molecules was found. A linear concentration dependence on 3-nitrotoluene and 4-nitro-m-xylene at micromolar concentrations was found during luminescent titration experiments (LOD values ca. 350 nM), suggesting this MOF to be a viable and highly sensitive luminescent sensor for such substrates.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/cryst14121026</doi><orcidid>https://orcid.org/0000-0001-8779-0612</orcidid><orcidid>https://orcid.org/0000-0001-5272-8878</orcidid><orcidid>https://orcid.org/0000-0001-8922-0066</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acids Analysis Coordination coordination polymers Crystallography Dimethylformamide Emission Ligands luminescence Metal-organic frameworks nitroaromatic Nitrotoluene Packing density Phosphorescence sensing Substrates Terbium terbium(III) Titration Topology Xylene |
title | Structures and Luminescent Sensing Properties of Terbium Metal–Organic Frameworks with Methyl-Decorated Phenanthroline Ligand |
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