A metal-organic framework constructed by a viologen-derived ligand: photochromism and discernible detection of volatile amine vapors

The detection of volatile amines has attracted great attention due to their high toxicity and widespread existence. Herein, we report a new example of a metal-organic framework (Co-MOF- 1 ) for the discriminative detection of alkylamines. Co-MOF- 1 that was assembled by Co( ii ), N 3 − and viologen-...

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Published inNew journal of chemistry Vol. 43; no. 23; pp. 932 - 938
Main Authors Dong, Zhen-Peng, Zhao, Jiao-Jiao, Liu, Peng-Yu, Liu, Zhi-Liang, Wang, Yan-Qin
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 10.06.2019
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Abstract The detection of volatile amines has attracted great attention due to their high toxicity and widespread existence. Herein, we report a new example of a metal-organic framework (Co-MOF- 1 ) for the discriminative detection of alkylamines. Co-MOF- 1 that was assembled by Co( ii ), N 3 − and viologen-based ligand [H 2 L]Cl 2 ([1,1′-bis(4-carboxylatobenzyl)-4,4′-bipyridinium] dichloride) is a 3D cationic pcu framework with 1D channels containing electron-deficient viologen units, exhibits typical electrochemical redox properties and photochromic properties, and is involved in the radical formation via photoinduced electron transfer from nitrate ions and carboxylate groups in the channels to viologen moieties. More importantly, Co-MOF- 1 shows different color responses to different volatile amine vapors of different types and molecular sizes, which is attributed to the electron transfer from the amine to viologen. Moreover, the reason why Co-MOF- 1 can detect amines distinguishably is the different sizes of the substituents of the amine molecules and the number of N-H bonds of the amine molecules. Furthermore, the portable test paper was successfully prepared and provided a convenient and discernible detection of volatile amine vapors by depositing Co-MOF- 1 onto the filter paper, which can also be used as an erasable inkless printing medium. A Co( ii )-MOF based on a viologen-derived ligand was obtained: the Co( ii ) compound exhibits photochromism, and allows the visual and differentiable detection of different volatile alkylamines.
AbstractList The detection of volatile amines has attracted great attention due to their high toxicity and widespread existence. Herein, we report a new example of a metal–organic framework (Co-MOF- 1 ) for the discriminative detection of alkylamines. Co-MOF- 1 that was assembled by Co( ii ), N 3 − and viologen-based ligand [H 2 L]Cl 2 ([1,1′-bis(4-carboxylatobenzyl)-4,4′-bipyridinium] dichloride) is a 3D cationic pcu framework with 1D channels containing electron-deficient viologen units, exhibits typical electrochemical redox properties and photochromic properties, and is involved in the radical formation via photoinduced electron transfer from nitrate ions and carboxylate groups in the channels to viologen moieties. More importantly, Co-MOF- 1 shows different color responses to different volatile amine vapors of different types and molecular sizes, which is attributed to the electron transfer from the amine to viologen. Moreover, the reason why Co-MOF- 1 can detect amines distinguishably is the different sizes of the substituents of the amine molecules and the number of N–H bonds of the amine molecules. Furthermore, the portable test paper was successfully prepared and provided a convenient and discernible detection of volatile amine vapors by depositing Co-MOF- 1 onto the filter paper, which can also be used as an erasable inkless printing medium.
The detection of volatile amines has attracted great attention due to their high toxicity and widespread existence. Herein, we report a new example of a metal–organic framework (Co-MOF-1) for the discriminative detection of alkylamines. Co-MOF-1 that was assembled by Co(ii), N3− and viologen-based ligand [H2L]Cl2 ([1,1′-bis(4-carboxylatobenzyl)-4,4′-bipyridinium] dichloride) is a 3D cationic pcu framework with 1D channels containing electron-deficient viologen units, exhibits typical electrochemical redox properties and photochromic properties, and is involved in the radical formation via photoinduced electron transfer from nitrate ions and carboxylate groups in the channels to viologen moieties. More importantly, Co-MOF-1 shows different color responses to different volatile amine vapors of different types and molecular sizes, which is attributed to the electron transfer from the amine to viologen. Moreover, the reason why Co-MOF-1 can detect amines distinguishably is the different sizes of the substituents of the amine molecules and the number of N–H bonds of the amine molecules. Furthermore, the portable test paper was successfully prepared and provided a convenient and discernible detection of volatile amine vapors by depositing Co-MOF-1 onto the filter paper, which can also be used as an erasable inkless printing medium.
The detection of volatile amines has attracted great attention due to their high toxicity and widespread existence. Herein, we report a new example of a metal-organic framework (Co-MOF- 1 ) for the discriminative detection of alkylamines. Co-MOF- 1 that was assembled by Co( ii ), N 3 − and viologen-based ligand [H 2 L]Cl 2 ([1,1′-bis(4-carboxylatobenzyl)-4,4′-bipyridinium] dichloride) is a 3D cationic pcu framework with 1D channels containing electron-deficient viologen units, exhibits typical electrochemical redox properties and photochromic properties, and is involved in the radical formation via photoinduced electron transfer from nitrate ions and carboxylate groups in the channels to viologen moieties. More importantly, Co-MOF- 1 shows different color responses to different volatile amine vapors of different types and molecular sizes, which is attributed to the electron transfer from the amine to viologen. Moreover, the reason why Co-MOF- 1 can detect amines distinguishably is the different sizes of the substituents of the amine molecules and the number of N-H bonds of the amine molecules. Furthermore, the portable test paper was successfully prepared and provided a convenient and discernible detection of volatile amine vapors by depositing Co-MOF- 1 onto the filter paper, which can also be used as an erasable inkless printing medium. A Co( ii )-MOF based on a viologen-derived ligand was obtained: the Co( ii ) compound exhibits photochromism, and allows the visual and differentiable detection of different volatile alkylamines.
Author Zhao, Jiao-Jiao
Liu, Peng-Yu
Liu, Zhi-Liang
Dong, Zhen-Peng
Wang, Yan-Qin
AuthorAffiliation Inner Mongolia Key Laboratory of Chemistry and Physics of Rare Earth Materials, College of Chemistry and Chemical Engineering, Inner Mongolia University
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Cites_doi 10.1021/jp0259869
10.1021/acs.inorgchem.7b02206
10.1021/acsami.9b00834
10.1002/chem.201704478
10.1021/acs.inorgchem.8b01141
10.1002/hlca.200590257
10.1039/C5QI00283D
10.1039/c3cc42268b
10.1021/acs.inorgchem.5b01651
10.1039/b807083k
10.1016/j.chroma.2012.05.094
10.1039/C5OB02211H
10.1002/bms.1200140505
10.1002/ejic.201501206
10.1039/C6CC10278F
10.1021/ic2020868
10.1039/C7TA05896A
10.1039/C4SC03224A
10.1002/anie.201609989
10.1021/acs.inorgchem.5b00023
10.1039/C6DT04108F
10.1016/j.trac.2015.09.006
10.1021/ja00227a062
10.1016/j.aca.2014.05.028
10.1021/ja4105478
10.1039/C6SC04579K
10.1021/acs.inorgchem.5b00975
10.1016/j.ccr.2017.10.029
10.1021/ja0111030
10.1021/ic50112a056
10.1039/C7DT00452D
10.1021/acsami.7b11125
10.1002/chem.201703253
10.1021/acs.jpclett.7b02452
10.1016/j.snb.2018.12.150
10.1039/b802426j
10.1016/j.trac.2017.11.001
10.1002/anie.200705545
10.1039/C8DT01034J
10.1016/j.snb.2004.11.054
10.1002/sia.740110607
10.1021/acsami.6b15540
10.1002/anie.201610180
10.1021/acsami.7b19356
10.1016/j.inoche.2015.06.008
10.1002/adma.201702298
10.1002/anie.201108220
10.1021/acsami.7b17381
10.1021/acs.cgd.8b00390
10.1002/cben.201600027
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References Chang (C9NJ01380F-(cit13)/*[position()=1]) 2012; 1248
Yoon (C9NJ01380F-(cit20a)/*[position()=1]) 1988; 110
Wang (C9NJ01380F-(cit25)/*[position()=1]) 2008; 47
Chowdhury (C9NJ01380F-(cit3)/*[position()=1]) 2017; 4
Yang (C9NJ01380F-(cit28c)/*[position()=1]) 2017; 53
Gong (C9NJ01380F-(cit22a)/*[position()=1]) 2013; 49
Gong (C9NJ01380F-(cit23c)/*[position()=1]) 2017; 9
Sui (C9NJ01380F-(cit17a)/*[position()=1]) 2018; 10
Liu (C9NJ01380F-(cit6d)/*[position()=1]) 2017; 46
Sui (C9NJ01380F-(cit16c)/*[position()=1]) 2017; 8
Illes (C9NJ01380F-(cit4)/*[position()=1]) 2018; 10
Alam (C9NJ01380F-(cit9a)/*[position()=1]) 2017; 23
Yang (C9NJ01380F-(cit27)/*[position()=1]) 2017; 46
Zhang (C9NJ01380F-(cit7b)/*[position()=1]) 2017; 9
Kan (C9NJ01380F-(cit16f)/*[position()=1]) 2017; 56
Fuchs (C9NJ01380F-(cit21b)/*[position()=1]) 2002; 106
Lawrence (C9NJ01380F-(cit8a)/*[position()=1]) 2004
Sajid (C9NJ01380F-(cit14)/*[position()=1]) 2016; 76
Sun (C9NJ01380F-(cit16d)/*[position()=1]) 2017; 56
Tan (C9NJ01380F-(cit18)/*[position()=1]) 2015; 58
Tao (C9NJ01380F-(cit20b)/*[position()=1]) 2016; 3
Finn (C9NJ01380F-(cit23a)/*[position()=1]) 1972; 11
Zhang (C9NJ01380F-(cit23b)/*[position()=1]) 2001; 123
Zhao (C9NJ01380F-(cit6b)/*[position()=1]) 2018; 47
Tan (C9NJ01380F-(cit28b)/*[position()=1]) 2015; 54
Valderrey (C9NJ01380F-(cit9b)/*[position()=1]) 2017; 56
Yang (C9NJ01380F-(cit28a)/*[position()=1]) 2018; 10
Gong (C9NJ01380F-(cit16e)/*[position()=1]) 2018; 57
Mallick (C9NJ01380F-(cit7a)/*[position()=1]) 2015; 6
Timmer (C9NJ01380F-(cit8b)/*[position()=1]) 2005; 107
Piasta (C9NJ01380F-(cit11)/*[position()=1]) 2014; 834
Sui (C9NJ01380F-(cit16a)/*[position()=1]) 2017; 8
Lv (C9NJ01380F-(cit22b)/*[position()=1]) 2012; 51
Liu (C9NJ01380F-(cit6c)/*[position()=1]) 2015; 54
Van Humbeck (C9NJ01380F-(cit7c)/*[position()=1]) 2014; 136
Ma (C9NJ01380F-(cit6a)/*[position()=1]) 2019; 11
Barth (C9NJ01380F-(cit24)/*[position()=1]) 1988; 11
Mallick (C9NJ01380F-(cit7d)/*[position()=1]) 2015; 6
Toma (C9NJ01380F-(cit21a)/*[position()=1]) 2016
Hu (C9NJ01380F-(cit16h)/*[position()=1]) 2017; 23
Xu (C9NJ01380F-(cit5a)/*[position()=1]) 2017; 29
Papageorgiou (C9NJ01380F-(cit10)/*[position()=1]) 2018; 98
Stillwell (C9NJ01380F-(cit12)/*[position()=1]) 1987; 14
Dong (C9NJ01380F-(cit5b)/*[position()=1]) 2019; 284
Yang (C9NJ01380F-(cit17b)/*[position()=1]) 2018; 18
Toma (C9NJ01380F-(cit26)/*[position()=1]) 2015; 54
Guo (C9NJ01380F-(cit5c)/*[position()=1]) 2017; 5
Chen (C9NJ01380F-(cit19a)/*[position()=1]) 2016; 14
Li (C9NJ01380F-(cit2)/*[position()=1]) 2009; 38
Bamfield (C9NJ01380F-(cit15b)/*[position()=1]) 2010
Ma (C9NJ01380F-(cit1)/*[position()=1]) 2009; 38
Sun (C9NJ01380F-(cit16b)/*[position()=1]) 2019; 378
Bongard (C9NJ01380F-(cit19b)/*[position()=1]) 2005; 88
Monk (C9NJ01380F-(cit15a)/*[position()=1]) 1999
Wang (C9NJ01380F-(cit16g)/*[position()=1]) 2012; 51
References_xml – issn: 1999
  publication-title: The Viologens: Physicochemical Properties, Synthesis and Applications of the Salts of 4,4′-Bipyridine
  doi: Monk
– issn: 2010
  publication-title: Chromic Phenomena: Technological Applications of Colour Chemistry
  doi: Bamfield Hutchings
– issn: 2004
  publication-title: Amines: Synthesis, Properties and Applications
  doi: Lawrence
– volume: 106
  start-page: 8885
  year: 2002
  ident: C9NJ01380F-(cit21b)/*[position()=1]
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp0259869
– volume: 56
  start-page: 14926
  year: 2017
  ident: C9NJ01380F-(cit16f)/*[position()=1]
  publication-title: Inorg. Chem.
  doi: 10.1021/acs.inorgchem.7b02206
– volume: 11
  start-page: 9233
  year: 2019
  ident: C9NJ01380F-(cit6a)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.9b00834
– volume: 23
  start-page: 18074
  year: 2017
  ident: C9NJ01380F-(cit16h)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201704478
– volume: 57
  start-page: 6791
  year: 2018
  ident: C9NJ01380F-(cit16e)/*[position()=1]
  publication-title: Inorg. Chem.
  doi: 10.1021/acs.inorgchem.8b01141
– volume: 88
  start-page: 3200
  year: 2005
  ident: C9NJ01380F-(cit19b)/*[position()=1]
  publication-title: Helv. Chim. Acta
  doi: 10.1002/hlca.200590257
– volume: 3
  start-page: 541
  year: 2016
  ident: C9NJ01380F-(cit20b)/*[position()=1]
  publication-title: Inorg. Chem. Front.
  doi: 10.1039/C5QI00283D
– volume: 49
  start-page: 7711
  year: 2013
  ident: C9NJ01380F-(cit22a)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/c3cc42268b
– volume: 54
  start-page: 8884
  year: 2015
  ident: C9NJ01380F-(cit6c)/*[position()=1]
  publication-title: Inorg. Chem.
  doi: 10.1021/acs.inorgchem.5b01651
– volume: 38
  start-page: 1248
  year: 2009
  ident: C9NJ01380F-(cit1)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/b807083k
– volume: 1248
  start-page: 41
  year: 2012
  ident: C9NJ01380F-(cit13)/*[position()=1]
  publication-title: J. Chromatogr. A
  doi: 10.1016/j.chroma.2012.05.094
– volume: 14
  start-page: 980
  year: 2016
  ident: C9NJ01380F-(cit19a)/*[position()=1]
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C5OB02211H
– volume: 14
  start-page: 221
  year: 1987
  ident: C9NJ01380F-(cit12)/*[position()=1]
  publication-title: Biomed. Environ. Mass Spectrom.
  doi: 10.1002/bms.1200140505
– start-page: 1036
  year: 2016
  ident: C9NJ01380F-(cit21a)/*[position()=1]
  publication-title: Eur. J. Inorg. Chem.
  doi: 10.1002/ejic.201501206
– volume: 53
  start-page: 1747
  year: 2017
  ident: C9NJ01380F-(cit28c)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C6CC10278F
– volume: 51
  start-page: 4015
  year: 2012
  ident: C9NJ01380F-(cit22b)/*[position()=1]
  publication-title: Inorg. Chem.
  doi: 10.1021/ic2020868
– volume: 5
  start-page: 20035
  year: 2017
  ident: C9NJ01380F-(cit5c)/*[position()=1]
  publication-title: J. Mater. Chem. A
  doi: 10.1039/C7TA05896A
– volume: 6
  start-page: 1420
  year: 2015
  ident: C9NJ01380F-(cit7d)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C4SC03224A
– volume: 56
  start-page: 1914
  year: 2017
  ident: C9NJ01380F-(cit9b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201609989
– volume: 54
  start-page: 3456
  year: 2015
  ident: C9NJ01380F-(cit28b)/*[position()=1]
  publication-title: Inorg. Chem.
  doi: 10.1021/acs.inorgchem.5b00023
– volume: 46
  start-page: 1207
  year: 2017
  ident: C9NJ01380F-(cit6d)/*[position()=1]
  publication-title: Dalton Trans.
  doi: 10.1039/C6DT04108F
– volume: 76
  start-page: 15
  year: 2016
  ident: C9NJ01380F-(cit14)/*[position()=1]
  publication-title: Trends Anal. Chem.
  doi: 10.1016/j.trac.2015.09.006
– volume-title: Chromic Phenomena: Technological Applications of Colour Chemistry
  year: 2010
  ident: C9NJ01380F-(cit15b)/*[position()=1]
– volume: 110
  start-page: 6586
  year: 1988
  ident: C9NJ01380F-(cit20a)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00227a062
– volume: 834
  start-page: 58
  year: 2014
  ident: C9NJ01380F-(cit11)/*[position()=1]
  publication-title: Anal. Chim. Acta
  doi: 10.1016/j.aca.2014.05.028
– volume-title: Amines: Synthesis, Properties and Applications
  year: 2004
  ident: C9NJ01380F-(cit8a)/*[position()=1]
– volume: 6
  start-page: 1420
  year: 2015
  ident: C9NJ01380F-(cit7a)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C4SC03224A
– volume: 136
  start-page: 2432
  year: 2014
  ident: C9NJ01380F-(cit7c)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja4105478
– volume-title: The Viologens: Physicochemical Properties, Synthesis and Applications of the Salts of 4,4′-Bipyridine
  year: 1999
  ident: C9NJ01380F-(cit15a)/*[position()=1]
– volume: 8
  start-page: 2758
  year: 2017
  ident: C9NJ01380F-(cit16c)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C6SC04579K
– volume: 54
  start-page: 8923
  year: 2015
  ident: C9NJ01380F-(cit26)/*[position()=1]
  publication-title: Inorg. Chem.
  doi: 10.1021/acs.inorgchem.5b00975
– volume: 378
  start-page: 533
  year: 2019
  ident: C9NJ01380F-(cit16b)/*[position()=1]
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/j.ccr.2017.10.029
– volume: 123
  start-page: 12105
  year: 2001
  ident: C9NJ01380F-(cit23b)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja0111030
– volume: 11
  start-page: 1434
  year: 1972
  ident: C9NJ01380F-(cit23a)/*[position()=1]
  publication-title: Inorg. Chem.
  doi: 10.1021/ic50112a056
– volume: 46
  start-page: 4366
  year: 2017
  ident: C9NJ01380F-(cit27)/*[position()=1]
  publication-title: Dalton Trans.
  doi: 10.1039/C7DT00452D
– volume: 9
  start-page: 31352
  year: 2017
  ident: C9NJ01380F-(cit7b)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.7b11125
– volume: 23
  start-page: 14911
  year: 2017
  ident: C9NJ01380F-(cit9a)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201703253
– volume: 8
  start-page: 5450
  year: 2017
  ident: C9NJ01380F-(cit16a)/*[position()=1]
  publication-title: J. Phys. Chem. Lett.
  doi: 10.1021/acs.jpclett.7b02452
– volume: 284
  start-page: 354
  year: 2019
  ident: C9NJ01380F-(cit5b)/*[position()=1]
  publication-title: Sens. Actuators, B
  doi: 10.1016/j.snb.2018.12.150
– volume: 38
  start-page: 1477
  year: 2009
  ident: C9NJ01380F-(cit2)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/b802426j
– volume: 98
  start-page: 128
  year: 2018
  ident: C9NJ01380F-(cit10)/*[position()=1]
  publication-title: TrAC, Trends Anal. Chem.
  doi: 10.1016/j.trac.2017.11.001
– volume: 47
  start-page: 3565
  year: 2008
  ident: C9NJ01380F-(cit25)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200705545
– volume: 47
  start-page: 8972
  year: 2018
  ident: C9NJ01380F-(cit6b)/*[position()=1]
  publication-title: Dalton Trans.
  doi: 10.1039/C8DT01034J
– volume: 107
  start-page: 666
  year: 2005
  ident: C9NJ01380F-(cit8b)/*[position()=1]
  publication-title: Sens. Actuators, B
  doi: 10.1016/j.snb.2004.11.054
– volume: 11
  start-page: 307
  year: 1988
  ident: C9NJ01380F-(cit24)/*[position()=1]
  publication-title: Surf. Interface Anal.
  doi: 10.1002/sia.740110607
– volume: 9
  start-page: 5503
  year: 2017
  ident: C9NJ01380F-(cit23c)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.6b15540
– volume: 56
  start-page: 554
  year: 2017
  ident: C9NJ01380F-(cit16d)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201610180
– volume: 10
  start-page: 12417
  year: 2018
  ident: C9NJ01380F-(cit4)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.7b19356
– volume: 58
  start-page: 67
  year: 2015
  ident: C9NJ01380F-(cit18)/*[position()=1]
  publication-title: Inorg. Chem. Commun.
  doi: 10.1016/j.inoche.2015.06.008
– volume: 29
  start-page: 1702298
  year: 2017
  ident: C9NJ01380F-(cit5a)/*[position()=1]
  publication-title: Adv. Mater.
  doi: 10.1002/adma.201702298
– volume: 51
  start-page: 3432
  year: 2012
  ident: C9NJ01380F-(cit16g)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201108220
– volume: 10
  start-page: 1105
  year: 2018
  ident: C9NJ01380F-(cit17a)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
– volume: 10
  start-page: 2735
  year: 2018
  ident: C9NJ01380F-(cit28a)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.7b17381
– volume: 18
  start-page: 3236
  year: 2018
  ident: C9NJ01380F-(cit17b)/*[position()=1]
  publication-title: Cryst. Growth Des.
  doi: 10.1021/acs.cgd.8b00390
– volume: 4
  start-page: 225
  year: 2017
  ident: C9NJ01380F-(cit3)/*[position()=1]
  publication-title: ChemBioEng Rev.
  doi: 10.1002/cben.201600027
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Snippet The detection of volatile amines has attracted great attention due to their high toxicity and widespread existence. Herein, we report a new example of a...
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SubjectTerms Alkylamines
Amines
Channels
Crystallography
Dichlorides
Electron transfer
Electrons
Filter paper
Ligands
Metal-organic frameworks
Photochromism
Toxicity
Title A metal-organic framework constructed by a viologen-derived ligand: photochromism and discernible detection of volatile amine vapors
URI https://www.proquest.com/docview/2237516078
Volume 43
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