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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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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. |
doi_str_mv | 10.1039/c4ce01791a |
format | article |
fullrecord | <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c4ce01791a</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c4ce01791a</sourcerecordid><originalsourceid>FETCH-rsc_primary_c4ce01791a3</originalsourceid><addsrcrecordid>eNqFUj1v2zAQVQsEaJp06V7gstmDXFFynThboCgfQDvRu3GizhYbihRIKoH_d35AaFmJNbUTCd577969YxR9Z8mMJdnyp5gLStjlkuHn6JTNF4v4KsmyL9FX5_4mCZszlpx-es3tznlUsTexOFzBW9RuY2yDXhrtAHUFbW28UV0jNTlBWhCIGvWWHEgNvibIu4mcgjDGVlL3RNDkX4x9clCiowrCC0Iv28geQ6DkNogXioS3RksBrmtbRQ1pj3YXpD9cwKTgj1PAZ5QKS0XXMBhXZmuxrQO3Qt_rQ1r1llOCyWqPBc6mM-C0bxN8lCYUFemtr12PZxhnOGAd8DTm84Bf3d8EGVQ7Fx7NZo9Kyxnc8hxatNiQJ3vkl0f-r747XwSN3-PAPvwNOatQgnTEBX4ZOKM0hNHeyrI7rOEddLUfpvgTF7ccLLlO-cHfYerRJMuDE5YERj7azHl0skHl6NtwnkU_7opV_hBbJ9atlU0If338PtlZdPGv-rqtNtn_NN4AAVPYtA</addsrcrecordid><sourcetype>Enrichment Source</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><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><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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source | Royal Society of Chemistry |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T16%3A29%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Crystal-to-crystal%20transformations%20and%20photoluminescence%20changes%20in%20the%20Cu(i)%20coordination%20networks%20based%20on%20a%20formamidinate%20ligandElectronic%20supplementary%20information%20(ESI)%20available:%20Crystallographic%20data%20for%202d%20and%202e%20(Table%20S1).%20Selected%20bond%20lengths%20for%201a-3a%20(Tables%20S2-S4).%20TGA%20analyses%20of%201a-2b.%20DSC%20parameters%20for%201a-3b%20(Tables%20S5%20and%20S6).%20Luminescence%20data%20for%20crystalline%202a-3b%20(Table%20S7).%20Electronic%20contributions%20(Table%20S8).%20SEM-EDS%20results%20of%201a%20and%202a%20(Tables%20S9%20and%20S10).%20Coordination&rft.au=Hsu,%20Wayne&rft.date=2014-11-02&rft.volume=16&rft.issue=46&rft.spage=164&rft.epage=1648&rft.pages=164-1648&rft.eissn=1466-8033&rft_id=info:doi/10.1039/c4ce01791a&rft_dat=%3Crsc%3Ec4ce01791a%3C/rsc%3E%3Cgrp_id%3Ecdi_FETCH-rsc_primary_c4ce01791a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |