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New hydrate cocrystal of l-proline with 4-acetylphenylboronic acid obtained via mechanochemistry and solvent evaporation: An experimental and theoretical study
In this work, we present the formation of a new multi-component molecular complex by targeting the boronic acid moiety (-B(OH)2) of 4-acetylphenylboronic acid with the carboxylate group (-COO-) of l-proline using two different techniques: mechanochemistry and solvent evaporation. The experiments pro...
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Published in: | Journal of solid state chemistry 2022-09, Vol.313, p.123282, Article 123282 |
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description | In this work, we present the formation of a new multi-component molecular complex by targeting the boronic acid moiety (-B(OH)2) of 4-acetylphenylboronic acid with the carboxylate group (-COO-) of l-proline using two different techniques: mechanochemistry and solvent evaporation. The experiments produced efficiently a new cocrystal named L-PRO4APBA. It was characterised to study its structural properties by X-ray powder diffraction (XRPD), infrared spectroscopy (FTIR), single-crystal X-ray diffraction (SCXRD), and quantum chemical methods based on QTAIM. Also, its thermal behaviour was analysed using a simultaneous DSC/TGA experiment. The results showed that L-PRO4APBA comprises discrete molecular units held together mainly by O–H⋯O and N–H⋯O hydrogen bonds. However, C–H⋯O, C–H⋯π, and other non-conventional interactions gave further stabilisation. Moreover, SCXRD showed that the asymmetric unit contains five independent molecules: two of l-proline (PRO1 and PRO2), two of 4-acetylphenylboronic acid (4APBA1 and 4APBA2) and one of water. PRO1 and PRO2 adopted different conformations with their carboxylate groups in equatorial and axial positions, respectively. This feature produced two independent helical chains running along the 21 screw axis in which 4APBA1 and 4APBA2 bound through the expected -B(OH)2···−OOC- heterosynthon. Surprisingly, the presence of water molecules in the lattice did not disrupt the formation of this motif. However, water molecules played an essential role for the stabilisation of the 3D structure. These findings would set up the structural basis to continue exploring the formation of new cocrystals by combining l-proline with boronic acids.
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•L-PRO4APBA cocrystal was obtained for the first time by mechanochemistry and solvent evaporation.•Surprisingly, lattice water molecules did not disrupt the -B(OH)2···−OOC- heterosynthon.•The work supports the basis for developing new stable cocrystals by combining l-proline with boronic acids.•Two independent helical chains were responsible for the compact non-centrosymmetric molecular packing.•C–O, B–O, and C–B bonds are stronger than those presented in tetracoordinate structures. |
doi_str_mv | 10.1016/j.jssc.2022.123282 |
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[Display omitted]
•L-PRO4APBA cocrystal was obtained for the first time by mechanochemistry and solvent evaporation.•Surprisingly, lattice water molecules did not disrupt the -B(OH)2···−OOC- heterosynthon.•The work supports the basis for developing new stable cocrystals by combining l-proline with boronic acids.•Two independent helical chains were responsible for the compact non-centrosymmetric molecular packing.•C–O, B–O, and C–B bonds are stronger than those presented in tetracoordinate structures.</description><identifier>ISSN: 0022-4596</identifier><identifier>EISSN: 1095-726X</identifier><identifier>DOI: 10.1016/j.jssc.2022.123282</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>Boron compound ; Cocrystal ; Hydrogen bond ; Mechanochemistry ; Proline ; QTAIM</subject><ispartof>Journal of solid state chemistry, 2022-09, Vol.313, p.123282, Article 123282</ispartof><rights>2022 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c230t-7e5381324951810942b40b4610e10d03490bbd894e53a0c15c65b2496210d58c3</citedby><cites>FETCH-LOGICAL-c230t-7e5381324951810942b40b4610e10d03490bbd894e53a0c15c65b2496210d58c3</cites><orcidid>0000-0001-5543-6889 ; 0000-0001-9720-9588</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></links><search><creatorcontrib>Hernández-Negrete, Ofelia</creatorcontrib><creatorcontrib>Sotelo-Mundo, Rogerio R.</creatorcontrib><creatorcontrib>Esparza-Ponce, Hilda E.</creatorcontrib><creatorcontrib>Encinas-Romero, Martín A.</creatorcontrib><creatorcontrib>Hernández-Paredes, Javier</creatorcontrib><title>New hydrate cocrystal of l-proline with 4-acetylphenylboronic acid obtained via mechanochemistry and solvent evaporation: An experimental and theoretical study</title><title>Journal of solid state chemistry</title><description>In this work, we present the formation of a new multi-component molecular complex by targeting the boronic acid moiety (-B(OH)2) of 4-acetylphenylboronic acid with the carboxylate group (-COO-) of l-proline using two different techniques: mechanochemistry and solvent evaporation. The experiments produced efficiently a new cocrystal named L-PRO4APBA. It was characterised to study its structural properties by X-ray powder diffraction (XRPD), infrared spectroscopy (FTIR), single-crystal X-ray diffraction (SCXRD), and quantum chemical methods based on QTAIM. Also, its thermal behaviour was analysed using a simultaneous DSC/TGA experiment. The results showed that L-PRO4APBA comprises discrete molecular units held together mainly by O–H⋯O and N–H⋯O hydrogen bonds. However, C–H⋯O, C–H⋯π, and other non-conventional interactions gave further stabilisation. Moreover, SCXRD showed that the asymmetric unit contains five independent molecules: two of l-proline (PRO1 and PRO2), two of 4-acetylphenylboronic acid (4APBA1 and 4APBA2) and one of water. PRO1 and PRO2 adopted different conformations with their carboxylate groups in equatorial and axial positions, respectively. This feature produced two independent helical chains running along the 21 screw axis in which 4APBA1 and 4APBA2 bound through the expected -B(OH)2···−OOC- heterosynthon. Surprisingly, the presence of water molecules in the lattice did not disrupt the formation of this motif. However, water molecules played an essential role for the stabilisation of the 3D structure. These findings would set up the structural basis to continue exploring the formation of new cocrystals by combining l-proline with boronic acids.
[Display omitted]
•L-PRO4APBA cocrystal was obtained for the first time by mechanochemistry and solvent evaporation.•Surprisingly, lattice water molecules did not disrupt the -B(OH)2···−OOC- heterosynthon.•The work supports the basis for developing new stable cocrystals by combining l-proline with boronic acids.•Two independent helical chains were responsible for the compact non-centrosymmetric molecular packing.•C–O, B–O, and C–B bonds are stronger than those presented in tetracoordinate structures.</description><subject>Boron compound</subject><subject>Cocrystal</subject><subject>Hydrogen bond</subject><subject>Mechanochemistry</subject><subject>Proline</subject><subject>QTAIM</subject><issn>0022-4596</issn><issn>1095-726X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9UMtOwzAQtBBIlMcPcPIPpNiOkyaIS4V4SRVcQOJmOeut4iq1I9sU8jX8Kq7KmdNqNTM7s0PIFWdzznh9vZlvYoS5YELMuShFI47IjLO2Khai_jgmM5aRQlZtfUrOYtwwxnnVyBn5ecEv2k8m6IQUPIQpJj1Qv6ZDMQY_WIf0y6aeykIDpmkYe3TT0PngnQWqwRrqu6Qzz9Cd1XSL0GvnocetjSlMVDtDox926BLFnR59trLe3dClo_g9YrDbDGXPPTH16AMmC3mP6dNMF-RkrYeIl3_znLw_3L_dPRWr18fnu-WqAFGyVCywKhteCtlWvMl_S9FJ1smaM-TMsFK2rOtM08rM0wx4BXXVZXYtMlw1UJ4TcbgLwccYcK3GHEyHSXGm9hWrjdpXrPYVq0PFWXR7EGFOtrMYVASLDtDYgJCU8fY_-S_QLYg3</recordid><startdate>202209</startdate><enddate>202209</enddate><creator>Hernández-Negrete, Ofelia</creator><creator>Sotelo-Mundo, Rogerio R.</creator><creator>Esparza-Ponce, Hilda E.</creator><creator>Encinas-Romero, Martín A.</creator><creator>Hernández-Paredes, Javier</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-5543-6889</orcidid><orcidid>https://orcid.org/0000-0001-9720-9588</orcidid></search><sort><creationdate>202209</creationdate><title>New hydrate cocrystal of l-proline with 4-acetylphenylboronic acid obtained via mechanochemistry and solvent evaporation: An experimental and theoretical study</title><author>Hernández-Negrete, Ofelia ; Sotelo-Mundo, Rogerio R. ; Esparza-Ponce, Hilda E. ; Encinas-Romero, Martín A. ; Hernández-Paredes, Javier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c230t-7e5381324951810942b40b4610e10d03490bbd894e53a0c15c65b2496210d58c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Boron compound</topic><topic>Cocrystal</topic><topic>Hydrogen bond</topic><topic>Mechanochemistry</topic><topic>Proline</topic><topic>QTAIM</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hernández-Negrete, Ofelia</creatorcontrib><creatorcontrib>Sotelo-Mundo, Rogerio R.</creatorcontrib><creatorcontrib>Esparza-Ponce, Hilda E.</creatorcontrib><creatorcontrib>Encinas-Romero, Martín A.</creatorcontrib><creatorcontrib>Hernández-Paredes, Javier</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of solid state chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hernández-Negrete, Ofelia</au><au>Sotelo-Mundo, Rogerio R.</au><au>Esparza-Ponce, Hilda E.</au><au>Encinas-Romero, Martín A.</au><au>Hernández-Paredes, Javier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New hydrate cocrystal of l-proline with 4-acetylphenylboronic acid obtained via mechanochemistry and solvent evaporation: An experimental and theoretical study</atitle><jtitle>Journal of solid state chemistry</jtitle><date>2022-09</date><risdate>2022</risdate><volume>313</volume><spage>123282</spage><pages>123282-</pages><artnum>123282</artnum><issn>0022-4596</issn><eissn>1095-726X</eissn><abstract>In this work, we present the formation of a new multi-component molecular complex by targeting the boronic acid moiety (-B(OH)2) of 4-acetylphenylboronic acid with the carboxylate group (-COO-) of l-proline using two different techniques: mechanochemistry and solvent evaporation. The experiments produced efficiently a new cocrystal named L-PRO4APBA. It was characterised to study its structural properties by X-ray powder diffraction (XRPD), infrared spectroscopy (FTIR), single-crystal X-ray diffraction (SCXRD), and quantum chemical methods based on QTAIM. Also, its thermal behaviour was analysed using a simultaneous DSC/TGA experiment. The results showed that L-PRO4APBA comprises discrete molecular units held together mainly by O–H⋯O and N–H⋯O hydrogen bonds. However, C–H⋯O, C–H⋯π, and other non-conventional interactions gave further stabilisation. Moreover, SCXRD showed that the asymmetric unit contains five independent molecules: two of l-proline (PRO1 and PRO2), two of 4-acetylphenylboronic acid (4APBA1 and 4APBA2) and one of water. PRO1 and PRO2 adopted different conformations with their carboxylate groups in equatorial and axial positions, respectively. This feature produced two independent helical chains running along the 21 screw axis in which 4APBA1 and 4APBA2 bound through the expected -B(OH)2···−OOC- heterosynthon. Surprisingly, the presence of water molecules in the lattice did not disrupt the formation of this motif. However, water molecules played an essential role for the stabilisation of the 3D structure. These findings would set up the structural basis to continue exploring the formation of new cocrystals by combining l-proline with boronic acids.
[Display omitted]
•L-PRO4APBA cocrystal was obtained for the first time by mechanochemistry and solvent evaporation.•Surprisingly, lattice water molecules did not disrupt the -B(OH)2···−OOC- heterosynthon.•The work supports the basis for developing new stable cocrystals by combining l-proline with boronic acids.•Two independent helical chains were responsible for the compact non-centrosymmetric molecular packing.•C–O, B–O, and C–B bonds are stronger than those presented in tetracoordinate structures.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.jssc.2022.123282</doi><orcidid>https://orcid.org/0000-0001-5543-6889</orcidid><orcidid>https://orcid.org/0000-0001-9720-9588</orcidid></addata></record> |
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subjects | Boron compound Cocrystal Hydrogen bond Mechanochemistry Proline QTAIM |
title | New hydrate cocrystal of l-proline with 4-acetylphenylboronic acid obtained via mechanochemistry and solvent evaporation: An experimental and theoretical study |
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