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Crystal-to-crystal transformations and photoluminescence changes in the Cu(i) coordination networks based on a formamidinate ligandElectronic supplementary information (ESI) available: Crystallographic data for 2d and 2e (Table S1). Selected bond lengths for 1a-3a (Tables S2-S4). TGA analyses of 1a-2b. DSC parameters for 1a-3b (Tables S5 and S6). Luminescence data for crystalline 2a-3b (Table S7). Electronic contributions (Table S8). SEM-EDS results of 1a and 2a (Tables S9 and S10). Coordination

One-pot solvothermal reactions of 4-aminopyridine and triethylorthoformate with Cu(O 2 CCH 3 ) 2 in acetone (ACT), dimethylformamide (DMF), tetrahydrofuran (THF), methanol (MeOH) and ethanol (EtOH) afforded 2D coordination networks, anti -{[Cu(4-pyf)]·ACT} n , 1a , (4-Hpyf = N , N′ -bis(pyridine-4-y...

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Main Authors: Hsu, Wayne, Chen, Kuan-Ting, Li, Yu-Sian, Cheng, Po-Wen, Chen, Tsun-Ren, Chen, Jhy-Der
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description One-pot solvothermal reactions of 4-aminopyridine and triethylorthoformate with Cu(O 2 CCH 3 ) 2 in acetone (ACT), dimethylformamide (DMF), tetrahydrofuran (THF), methanol (MeOH) and ethanol (EtOH) afforded 2D coordination networks, anti -{[Cu(4-pyf)]·ACT} n , 1a , (4-Hpyf = N , N′ -bis(pyridine-4-yl)formamidine), anti -{[Cu(4-pyf)]·DMF} n , 1b , anti -{[Cu(4-pyf)]·THF]} n , 1c , syn -{[Cu 4 (4-pyf) 4 ]·2MeOH} n , 2a , and syn -{[Cu 4 (4-pyf) 4 ]·2EtOH} n , 2b , whereas the reaction of Cu(O 2 CCH 3 ) 2 , 4-aminopyridine, triethylorthoformate and CuX 2 (X = BF 4 − and ClO 4 − ) in ethanol gave the 3D coordination networks syn -{[Cu 3 (4-pyf) 2 ](BF 4 )·2H 2 O·EtOH} n , 3a , and syn -{[Cu 3 (4-pyf) 2 ](ClO 4 )·EtOH} n , 3b , which were characterized by X-ray crystallography. Complexes 1a-3b are the first 2D and 3D coordination networks showing closed-shell Cu( i )-Cu( i ) interactions that are supported by the formamidinate ligands. Reversible crystal-to-crystal transformations were observed for the 2D anti - and syn -coordination networks upon solvent exchange. Irreversible anti to syn crystal-to-crystal transformations can be shown upon solvent removal and the important intermediate, syn -{[Cu 4 (4-pyf) 4 ]·2THF} n , 2c , which verifies the temperature-dependent transformation, was structurally characterized. The configurations of the structures have significant influence on the emission properties. While the syn -complexes show broad emission bands, those of the anti -complexes are not detectable, indicating that cuprophilicity is unlikely to play significant roles in determining the emission of 1a-3b . The 2D anti - and syn -complexes that show outwardly dangling pyridyl rings may adsorb Cd salts through Cd-N interactions. While the syn -complexes show broad emission bands, those of the anti -complexes are not detectable, indicating that cuprophilicity is unlikely to play a significant role in determining the emission.
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Selected bond lengths for 1a-3a (Tables S2-S4). TGA analyses of 1a-2b. DSC parameters for 1a-3b (Tables S5 and S6). Luminescence data for crystalline 2a-3b (Table S7). Electronic contributions (Table S8). SEM-EDS results of 1a and 2a (Tables S9 and S10). Coordination</title><source>Royal Society of Chemistry</source><creator>Hsu, Wayne ; Chen, Kuan-Ting ; Li, Yu-Sian ; Cheng, Po-Wen ; Chen, Tsun-Ren ; Chen, Jhy-Der</creator><creatorcontrib>Hsu, Wayne ; Chen, Kuan-Ting ; Li, Yu-Sian ; Cheng, Po-Wen ; Chen, Tsun-Ren ; Chen, Jhy-Der</creatorcontrib><description>One-pot solvothermal reactions of 4-aminopyridine and triethylorthoformate with Cu(O 2 CCH 3 ) 2 in acetone (ACT), dimethylformamide (DMF), tetrahydrofuran (THF), methanol (MeOH) and ethanol (EtOH) afforded 2D coordination networks, anti -{[Cu(4-pyf)]·ACT} n , 1a , (4-Hpyf = N , N′ -bis(pyridine-4-yl)formamidine), anti -{[Cu(4-pyf)]·DMF} n , 1b , anti -{[Cu(4-pyf)]·THF]} n , 1c , syn -{[Cu 4 (4-pyf) 4 ]·2MeOH} n , 2a , and syn -{[Cu 4 (4-pyf) 4 ]·2EtOH} n , 2b , whereas the reaction of Cu(O 2 CCH 3 ) 2 , 4-aminopyridine, triethylorthoformate and CuX 2 (X = BF 4 − and ClO 4 − ) in ethanol gave the 3D coordination networks syn -{[Cu 3 (4-pyf) 2 ](BF 4 )·2H 2 O·EtOH} n , 3a , and syn -{[Cu 3 (4-pyf) 2 ](ClO 4 )·EtOH} n , 3b , which were characterized by X-ray crystallography. Complexes 1a-3b are the first 2D and 3D coordination networks showing closed-shell Cu( i )-Cu( i ) interactions that are supported by the formamidinate ligands. Reversible crystal-to-crystal transformations were observed for the 2D anti - and syn -coordination networks upon solvent exchange. Irreversible anti to syn crystal-to-crystal transformations can be shown upon solvent removal and the important intermediate, syn -{[Cu 4 (4-pyf) 4 ]·2THF} n , 2c , which verifies the temperature-dependent transformation, was structurally characterized. The configurations of the structures have significant influence on the emission properties. While the syn -complexes show broad emission bands, those of the anti -complexes are not detectable, indicating that cuprophilicity is unlikely to play significant roles in determining the emission of 1a-3b . The 2D anti - and syn -complexes that show outwardly dangling pyridyl rings may adsorb Cd salts through Cd-N interactions. While the syn -complexes show broad emission bands, those of the anti -complexes are not detectable, indicating that cuprophilicity is unlikely to play a significant role in determining the emission.</description><identifier>EISSN: 1466-8033</identifier><identifier>DOI: 10.1039/c4ce01791a</identifier><language>eng</language><creationdate>2014-11</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Hsu, Wayne</creatorcontrib><creatorcontrib>Chen, Kuan-Ting</creatorcontrib><creatorcontrib>Li, Yu-Sian</creatorcontrib><creatorcontrib>Cheng, Po-Wen</creatorcontrib><creatorcontrib>Chen, Tsun-Ren</creatorcontrib><creatorcontrib>Chen, Jhy-Der</creatorcontrib><title>Crystal-to-crystal transformations and photoluminescence changes in the Cu(i) coordination networks based on a formamidinate ligandElectronic supplementary information (ESI) available: Crystallographic data for 2d and 2e (Table S1). Selected bond lengths for 1a-3a (Tables S2-S4). TGA analyses of 1a-2b. DSC parameters for 1a-3b (Tables S5 and S6). Luminescence data for crystalline 2a-3b (Table S7). Electronic contributions (Table S8). SEM-EDS results of 1a and 2a (Tables S9 and S10). Coordination</title><description>One-pot solvothermal reactions of 4-aminopyridine and triethylorthoformate with Cu(O 2 CCH 3 ) 2 in acetone (ACT), dimethylformamide (DMF), tetrahydrofuran (THF), methanol (MeOH) and ethanol (EtOH) afforded 2D coordination networks, anti -{[Cu(4-pyf)]·ACT} n , 1a , (4-Hpyf = N , N′ -bis(pyridine-4-yl)formamidine), anti -{[Cu(4-pyf)]·DMF} n , 1b , anti -{[Cu(4-pyf)]·THF]} n , 1c , syn -{[Cu 4 (4-pyf) 4 ]·2MeOH} n , 2a , and syn -{[Cu 4 (4-pyf) 4 ]·2EtOH} n , 2b , whereas the reaction of Cu(O 2 CCH 3 ) 2 , 4-aminopyridine, triethylorthoformate and CuX 2 (X = BF 4 − and ClO 4 − ) in ethanol gave the 3D coordination networks syn -{[Cu 3 (4-pyf) 2 ](BF 4 )·2H 2 O·EtOH} n , 3a , and syn -{[Cu 3 (4-pyf) 2 ](ClO 4 )·EtOH} n , 3b , which were characterized by X-ray crystallography. Complexes 1a-3b are the first 2D and 3D coordination networks showing closed-shell Cu( i )-Cu( i ) interactions that are supported by the formamidinate ligands. Reversible crystal-to-crystal transformations were observed for the 2D anti - and syn -coordination networks upon solvent exchange. Irreversible anti to syn crystal-to-crystal transformations can be shown upon solvent removal and the important intermediate, syn -{[Cu 4 (4-pyf) 4 ]·2THF} n , 2c , which verifies the temperature-dependent transformation, was structurally characterized. The configurations of the structures have significant influence on the emission properties. While the syn -complexes show broad emission bands, those of the anti -complexes are not detectable, indicating that cuprophilicity is unlikely to play significant roles in determining the emission of 1a-3b . The 2D anti - and syn -complexes that show outwardly dangling pyridyl rings may adsorb Cd salts through Cd-N interactions. While the syn -complexes show broad emission bands, those of the anti -complexes are not detectable, indicating that cuprophilicity is unlikely to play a significant role in determining the emission.</description><issn>1466-8033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFUj1v2zAQVQsEaJp06V7gstmDXFFynThboCgfQDvRu3GizhYbihRIKoH_d35AaFmJNbUTCd577969YxR9Z8mMJdnyp5gLStjlkuHn6JTNF4v4KsmyL9FX5_4mCZszlpx-es3tznlUsTexOFzBW9RuY2yDXhrtAHUFbW28UV0jNTlBWhCIGvWWHEgNvibIu4mcgjDGVlL3RNDkX4x9clCiowrCC0Iv28geQ6DkNogXioS3RksBrmtbRQ1pj3YXpD9cwKTgj1PAZ5QKS0XXMBhXZmuxrQO3Qt_rQ1r1llOCyWqPBc6mM-C0bxN8lCYUFemtr12PZxhnOGAd8DTm84Bf3d8EGVQ7Fx7NZo9Kyxnc8hxatNiQJ3vkl0f-r747XwSN3-PAPvwNOatQgnTEBX4ZOKM0hNHeyrI7rOEddLUfpvgTF7ccLLlO-cHfYerRJMuDE5YERj7azHl0skHl6NtwnkU_7opV_hBbJ9atlU0If338PtlZdPGv-rqtNtn_NN4AAVPYtA</recordid><startdate>20141102</startdate><enddate>20141102</enddate><creator>Hsu, Wayne</creator><creator>Chen, Kuan-Ting</creator><creator>Li, Yu-Sian</creator><creator>Cheng, Po-Wen</creator><creator>Chen, Tsun-Ren</creator><creator>Chen, Jhy-Der</creator><scope/></search><sort><creationdate>20141102</creationdate><title>Crystal-to-crystal transformations and photoluminescence changes in the Cu(i) coordination networks based on a formamidinate ligandElectronic supplementary information (ESI) available: Crystallographic data for 2d and 2e (Table S1). Selected bond lengths for 1a-3a (Tables S2-S4). TGA analyses of 1a-2b. DSC parameters for 1a-3b (Tables S5 and S6). Luminescence data for crystalline 2a-3b (Table S7). Electronic contributions (Table S8). SEM-EDS results of 1a and 2a (Tables S9 and S10). Coordination</title><author>Hsu, Wayne ; Chen, Kuan-Ting ; Li, Yu-Sian ; Cheng, Po-Wen ; Chen, Tsun-Ren ; Chen, Jhy-Der</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c4ce01791a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hsu, Wayne</creatorcontrib><creatorcontrib>Chen, Kuan-Ting</creatorcontrib><creatorcontrib>Li, Yu-Sian</creatorcontrib><creatorcontrib>Cheng, Po-Wen</creatorcontrib><creatorcontrib>Chen, Tsun-Ren</creatorcontrib><creatorcontrib>Chen, Jhy-Der</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hsu, Wayne</au><au>Chen, Kuan-Ting</au><au>Li, Yu-Sian</au><au>Cheng, Po-Wen</au><au>Chen, Tsun-Ren</au><au>Chen, Jhy-Der</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Crystal-to-crystal transformations and photoluminescence changes in the Cu(i) coordination networks based on a formamidinate ligandElectronic supplementary information (ESI) available: Crystallographic data for 2d and 2e (Table S1). Selected bond lengths for 1a-3a (Tables S2-S4). TGA analyses of 1a-2b. DSC parameters for 1a-3b (Tables S5 and S6). Luminescence data for crystalline 2a-3b (Table S7). Electronic contributions (Table S8). SEM-EDS results of 1a and 2a (Tables S9 and S10). Coordination</atitle><date>2014-11-02</date><risdate>2014</risdate><volume>16</volume><issue>46</issue><spage>164</spage><epage>1648</epage><pages>164-1648</pages><eissn>1466-8033</eissn><abstract>One-pot solvothermal reactions of 4-aminopyridine and triethylorthoformate with Cu(O 2 CCH 3 ) 2 in acetone (ACT), dimethylformamide (DMF), tetrahydrofuran (THF), methanol (MeOH) and ethanol (EtOH) afforded 2D coordination networks, anti -{[Cu(4-pyf)]·ACT} n , 1a , (4-Hpyf = N , N′ -bis(pyridine-4-yl)formamidine), anti -{[Cu(4-pyf)]·DMF} n , 1b , anti -{[Cu(4-pyf)]·THF]} n , 1c , syn -{[Cu 4 (4-pyf) 4 ]·2MeOH} n , 2a , and syn -{[Cu 4 (4-pyf) 4 ]·2EtOH} n , 2b , whereas the reaction of Cu(O 2 CCH 3 ) 2 , 4-aminopyridine, triethylorthoformate and CuX 2 (X = BF 4 − and ClO 4 − ) in ethanol gave the 3D coordination networks syn -{[Cu 3 (4-pyf) 2 ](BF 4 )·2H 2 O·EtOH} n , 3a , and syn -{[Cu 3 (4-pyf) 2 ](ClO 4 )·EtOH} n , 3b , which were characterized by X-ray crystallography. Complexes 1a-3b are the first 2D and 3D coordination networks showing closed-shell Cu( i )-Cu( i ) interactions that are supported by the formamidinate ligands. Reversible crystal-to-crystal transformations were observed for the 2D anti - and syn -coordination networks upon solvent exchange. Irreversible anti to syn crystal-to-crystal transformations can be shown upon solvent removal and the important intermediate, syn -{[Cu 4 (4-pyf) 4 ]·2THF} n , 2c , which verifies the temperature-dependent transformation, was structurally characterized. The configurations of the structures have significant influence on the emission properties. While the syn -complexes show broad emission bands, those of the anti -complexes are not detectable, indicating that cuprophilicity is unlikely to play significant roles in determining the emission of 1a-3b . The 2D anti - and syn -complexes that show outwardly dangling pyridyl rings may adsorb Cd salts through Cd-N interactions. While the syn -complexes show broad emission bands, those of the anti -complexes are not detectable, indicating that cuprophilicity is unlikely to play a significant role in determining the emission.</abstract><doi>10.1039/c4ce01791a</doi><tpages>9</tpages></addata></record>
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title Crystal-to-crystal transformations and photoluminescence changes in the Cu(i) coordination networks based on a formamidinate ligandElectronic supplementary information (ESI) available: Crystallographic data for 2d and 2e (Table S1). Selected bond lengths for 1a-3a (Tables S2-S4). TGA analyses of 1a-2b. DSC parameters for 1a-3b (Tables S5 and S6). Luminescence data for crystalline 2a-3b (Table S7). Electronic contributions (Table S8). SEM-EDS results of 1a and 2a (Tables S9 and S10). Coordination
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