Luminescent organoboron compounds derived from salicylidenebenzohydrazide: Synthesis, characterization, structure, and photophysical properties
A series of substituted 2-hydroxysalicylidine benzohydrazides were converted into their phenyl-boron complexes in good yields upon reaction with phenylboronic acid. All new compounds were characterized by NMR, UV, IR, spectroscopy and mass spectrometry. The X-ray structures of two complexes demonstr...
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Veröffentlicht in: | Dyes and pigments 2013-12, Vol.99 (3), p.1036-1043 |
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creator | Chan-Navarro, Rodrigo Jiménez-Pérez, Víctor M. Muñoz-Flores, Blanca M. Dias, H.V. Rasika Moggio, Ivana Arias, Eduardo Ramos-Ortíz, Gabriel Santillan, Rosa García, Concepción Ochoa, Maria Eugenia Yousufuddin, Muhammed Waksman, Noemi |
description | A series of substituted 2-hydroxysalicylidine benzohydrazides were converted into their phenyl-boron complexes in good yields upon reaction with phenylboronic acid. All new compounds were characterized by NMR, UV, IR, spectroscopy and mass spectrometry. The X-ray structures of two complexes demonstrate that the boron atoms adopt a tetrahedral geometry. The 11B NMR chemical shifts of the boron atom in the complexes are also consistent with the presence of tetracoordinate boron centres. The photophysical properties of the free benzohydrazide ligands and their boron complexes have been determined and display quantum yields below 1% with lifetimes in the range 10−10–10−11 s.
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•Synthesis and photophysical properties of new organoboron compounds derived from salicylidenebenzohydrazide.•Push–pull model of boron complexes bonded to tridentate ONO ligands.•Non-planar molecular structures determined by X-ray crystallography. |
doi_str_mv | 10.1016/j.dyepig.2013.07.039 |
format | Article |
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[Display omitted]
•Synthesis and photophysical properties of new organoboron compounds derived from salicylidenebenzohydrazide.•Push–pull model of boron complexes bonded to tridentate ONO ligands.•Non-planar molecular structures determined by X-ray crystallography.</description><identifier>ISSN: 0143-7208</identifier><identifier>EISSN: 1873-3743</identifier><identifier>DOI: 10.1016/j.dyepig.2013.07.039</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>11B-NMR ; Atomic structure ; Boron ; Dyes ; Fluorescent ; Infrared radiation ; Ligands ; Nuclear magnetic resonance ; Organic materials ; Organoboron compounds ; Salicylidenebenzohydrazide ; X-ray ; X-rays</subject><ispartof>Dyes and pigments, 2013-12, Vol.99 (3), p.1036-1043</ispartof><rights>2013 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-b4a29c5fd7212d872204f2b0132588b2fc906a7c7f15bbaa24fdbc341eb5fde73</citedby><cites>FETCH-LOGICAL-c372t-b4a29c5fd7212d872204f2b0132588b2fc906a7c7f15bbaa24fdbc341eb5fde73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0143720813002982$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids></links><search><creatorcontrib>Chan-Navarro, Rodrigo</creatorcontrib><creatorcontrib>Jiménez-Pérez, Víctor M.</creatorcontrib><creatorcontrib>Muñoz-Flores, Blanca M.</creatorcontrib><creatorcontrib>Dias, H.V. Rasika</creatorcontrib><creatorcontrib>Moggio, Ivana</creatorcontrib><creatorcontrib>Arias, Eduardo</creatorcontrib><creatorcontrib>Ramos-Ortíz, Gabriel</creatorcontrib><creatorcontrib>Santillan, Rosa</creatorcontrib><creatorcontrib>García, Concepción</creatorcontrib><creatorcontrib>Ochoa, Maria Eugenia</creatorcontrib><creatorcontrib>Yousufuddin, Muhammed</creatorcontrib><creatorcontrib>Waksman, Noemi</creatorcontrib><title>Luminescent organoboron compounds derived from salicylidenebenzohydrazide: Synthesis, characterization, structure, and photophysical properties</title><title>Dyes and pigments</title><description>A series of substituted 2-hydroxysalicylidine benzohydrazides were converted into their phenyl-boron complexes in good yields upon reaction with phenylboronic acid. All new compounds were characterized by NMR, UV, IR, spectroscopy and mass spectrometry. The X-ray structures of two complexes demonstrate that the boron atoms adopt a tetrahedral geometry. The 11B NMR chemical shifts of the boron atom in the complexes are also consistent with the presence of tetracoordinate boron centres. The photophysical properties of the free benzohydrazide ligands and their boron complexes have been determined and display quantum yields below 1% with lifetimes in the range 10−10–10−11 s.
[Display omitted]
•Synthesis and photophysical properties of new organoboron compounds derived from salicylidenebenzohydrazide.•Push–pull model of boron complexes bonded to tridentate ONO ligands.•Non-planar molecular structures determined by X-ray crystallography.</description><subject>11B-NMR</subject><subject>Atomic structure</subject><subject>Boron</subject><subject>Dyes</subject><subject>Fluorescent</subject><subject>Infrared radiation</subject><subject>Ligands</subject><subject>Nuclear magnetic resonance</subject><subject>Organic materials</subject><subject>Organoboron compounds</subject><subject>Salicylidenebenzohydrazide</subject><subject>X-ray</subject><subject>X-rays</subject><issn>0143-7208</issn><issn>1873-3743</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1DAUhS0EEkPLG7DwksUk9U8yTlggoYoWpJFYFNaWf24ajxI72E6lzEvwyrga1nR1daXznatzD0IfKKkpoYebU203WNxjzQjlNRE14f0rtKOd4BUXDX-NdoQ2vBKMdG_Ru5ROhJCOM7pDf47r7DwkAz7jEB-VDzrE4LEJ8xJWbxO2EN0TWDzEMOOkJme2yVnwoMGfw7jZqM5l_4QfNp9HSC7tsRlVVCYX8qyyC36PU46ryWuEPVbe4mUMOSzjlpxRE15iWCBmB-kavRnUlOD9v3mFft19_Xn7rTr-uP9---VYGS5YrnSjWG_awQpGme0EY6QZmC7xWdt1mg2mJwcljBhoq7VSrBmsNryhoAsEgl-hjxffcvr3CinL2ZUnTJPyENYkqTgw2pC2OL4obTnpRU9pV6TNRWpiSCnCIJfoZhU3SYl8rkqe5KUq-VyVJEKWqgr2-YJBSfzkIMpkHHgD1kUwWdrg_m_wF2sRpC0</recordid><startdate>20131201</startdate><enddate>20131201</enddate><creator>Chan-Navarro, Rodrigo</creator><creator>Jiménez-Pérez, Víctor M.</creator><creator>Muñoz-Flores, Blanca M.</creator><creator>Dias, H.V. Rasika</creator><creator>Moggio, Ivana</creator><creator>Arias, Eduardo</creator><creator>Ramos-Ortíz, Gabriel</creator><creator>Santillan, Rosa</creator><creator>García, Concepción</creator><creator>Ochoa, Maria Eugenia</creator><creator>Yousufuddin, Muhammed</creator><creator>Waksman, Noemi</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20131201</creationdate><title>Luminescent organoboron compounds derived from salicylidenebenzohydrazide: Synthesis, characterization, structure, and photophysical properties</title><author>Chan-Navarro, Rodrigo ; Jiménez-Pérez, Víctor M. ; Muñoz-Flores, Blanca M. ; Dias, H.V. Rasika ; Moggio, Ivana ; Arias, Eduardo ; Ramos-Ortíz, Gabriel ; Santillan, Rosa ; García, Concepción ; Ochoa, Maria Eugenia ; Yousufuddin, Muhammed ; Waksman, Noemi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-b4a29c5fd7212d872204f2b0132588b2fc906a7c7f15bbaa24fdbc341eb5fde73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>11B-NMR</topic><topic>Atomic structure</topic><topic>Boron</topic><topic>Dyes</topic><topic>Fluorescent</topic><topic>Infrared radiation</topic><topic>Ligands</topic><topic>Nuclear magnetic resonance</topic><topic>Organic materials</topic><topic>Organoboron compounds</topic><topic>Salicylidenebenzohydrazide</topic><topic>X-ray</topic><topic>X-rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chan-Navarro, Rodrigo</creatorcontrib><creatorcontrib>Jiménez-Pérez, Víctor M.</creatorcontrib><creatorcontrib>Muñoz-Flores, Blanca M.</creatorcontrib><creatorcontrib>Dias, H.V. Rasika</creatorcontrib><creatorcontrib>Moggio, Ivana</creatorcontrib><creatorcontrib>Arias, Eduardo</creatorcontrib><creatorcontrib>Ramos-Ortíz, Gabriel</creatorcontrib><creatorcontrib>Santillan, Rosa</creatorcontrib><creatorcontrib>García, Concepción</creatorcontrib><creatorcontrib>Ochoa, Maria Eugenia</creatorcontrib><creatorcontrib>Yousufuddin, Muhammed</creatorcontrib><creatorcontrib>Waksman, Noemi</creatorcontrib><collection>CrossRef</collection><collection>Ceramic Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Dyes and pigments</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chan-Navarro, Rodrigo</au><au>Jiménez-Pérez, Víctor M.</au><au>Muñoz-Flores, Blanca M.</au><au>Dias, H.V. Rasika</au><au>Moggio, Ivana</au><au>Arias, Eduardo</au><au>Ramos-Ortíz, Gabriel</au><au>Santillan, Rosa</au><au>García, Concepción</au><au>Ochoa, Maria Eugenia</au><au>Yousufuddin, Muhammed</au><au>Waksman, Noemi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Luminescent organoboron compounds derived from salicylidenebenzohydrazide: Synthesis, characterization, structure, and photophysical properties</atitle><jtitle>Dyes and pigments</jtitle><date>2013-12-01</date><risdate>2013</risdate><volume>99</volume><issue>3</issue><spage>1036</spage><epage>1043</epage><pages>1036-1043</pages><issn>0143-7208</issn><eissn>1873-3743</eissn><abstract>A series of substituted 2-hydroxysalicylidine benzohydrazides were converted into their phenyl-boron complexes in good yields upon reaction with phenylboronic acid. All new compounds were characterized by NMR, UV, IR, spectroscopy and mass spectrometry. The X-ray structures of two complexes demonstrate that the boron atoms adopt a tetrahedral geometry. The 11B NMR chemical shifts of the boron atom in the complexes are also consistent with the presence of tetracoordinate boron centres. The photophysical properties of the free benzohydrazide ligands and their boron complexes have been determined and display quantum yields below 1% with lifetimes in the range 10−10–10−11 s.
[Display omitted]
•Synthesis and photophysical properties of new organoboron compounds derived from salicylidenebenzohydrazide.•Push–pull model of boron complexes bonded to tridentate ONO ligands.•Non-planar molecular structures determined by X-ray crystallography.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.dyepig.2013.07.039</doi><tpages>8</tpages></addata></record> |
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subjects | 11B-NMR Atomic structure Boron Dyes Fluorescent Infrared radiation Ligands Nuclear magnetic resonance Organic materials Organoboron compounds Salicylidenebenzohydrazide X-ray X-rays |
title | Luminescent organoboron compounds derived from salicylidenebenzohydrazide: Synthesis, characterization, structure, and photophysical properties |
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