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-...
Saved in:
Published in | New journal of chemistry Vol. 43; no. 23; pp. 932 - 938 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
10.06.2019
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
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 |
AuthorAffiliation_xml | – name: Inner Mongolia Key Laboratory of Chemistry and Physics of Rare Earth Materials, College of Chemistry and Chemical Engineering, Inner Mongolia University |
Author_xml | – sequence: 1 givenname: Zhen-Peng surname: Dong fullname: Dong, Zhen-Peng – sequence: 2 givenname: Jiao-Jiao surname: Zhao fullname: Zhao, Jiao-Jiao – sequence: 3 givenname: Peng-Yu surname: Liu fullname: Liu, Peng-Yu – sequence: 4 givenname: Zhi-Liang surname: Liu fullname: Liu, Zhi-Liang – sequence: 5 givenname: Yan-Qin surname: Wang fullname: Wang, Yan-Qin |
BookMark | eNp9kUtr3TAQhUVJIK9usi8odFdwq4dt2dmFS9MHIdm0azOWRolubcmRdG_JPj88Sm9pIZSuZjh8Z4Y5c0T2fPBIyCln7zmT_Qfd-zXjsmP2FTnksu2rXrR8r_S8rivW1O0BOUppzRjnquWH5PGCzphhqkK8Be80tRFm_BniD6qDTzludEZDxwcKdOvCFG7RVwaj2xZ1csVjzulyF3LQdzHMLs20SNS4pDF6N05IDWbU2QVPg6XbMEF2RYXZeaRbWEJMJ2TfwpTw9e96TL5ffvy2-lxd3Xz6srq4qrRkKlcdg9GqBkdoJK8N1sCtEkYJa4XRraxr6HgrO4G17hhnRggN2hhQrDfNqOQxebubu8Rwv8GUh3XYRF9WDkJI1fCWqa5QbEfpGFKKaAftMjwfkCO4aeBseM56WPXXX39lfVks715YluhmiA__hs92cEz6D_f3ccNibGHe_I-RT4tNmYs |
CitedBy_id | crossref_primary_10_1021_acs_cgd_2c00016 crossref_primary_10_1002_slct_202300478 crossref_primary_10_1002_aoc_5477 crossref_primary_10_1002_slct_202400788 crossref_primary_10_1016_j_jssc_2022_122889 crossref_primary_10_1016_j_jssc_2020_121755 crossref_primary_10_1016_j_colsurfa_2024_133161 crossref_primary_10_1002_smll_202405176 crossref_primary_10_1039_D1RA01151K crossref_primary_10_1016_j_ccr_2021_213955 crossref_primary_10_1021_acs_inorgchem_1c03203 crossref_primary_10_3390_molecules26206209 crossref_primary_10_1016_j_jphotochem_2023_115262 crossref_primary_10_1016_j_seppur_2021_120246 crossref_primary_10_1016_j_jhazmat_2022_129364 crossref_primary_10_1016_j_poly_2023_116796 crossref_primary_10_1039_D1NJ06158E crossref_primary_10_1002_cplu_202200171 crossref_primary_10_1021_acsami_9b17391 crossref_primary_10_1039_D0CE01630F crossref_primary_10_1016_j_ccr_2024_216064 crossref_primary_10_1021_acs_cgd_0c01113 crossref_primary_10_1039_D3TC01624B crossref_primary_10_1002_ejic_202200672 crossref_primary_10_1016_j_ijbiomac_2024_139308 crossref_primary_10_1016_j_inoche_2023_111078 crossref_primary_10_1039_D0MA00038H crossref_primary_10_1039_D2DT02792E crossref_primary_10_1016_j_inoche_2024_113239 crossref_primary_10_1016_j_inoche_2024_112725 crossref_primary_10_1039_D1NJ04918F |
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 |
ContentType | Journal Article |
Copyright | Copyright Royal Society of Chemistry 2019 |
Copyright_xml | – notice: Copyright Royal Society of Chemistry 2019 |
DBID | AAYXX CITATION 7SR 8BQ 8FD H9R JG9 KA0 |
DOI | 10.1039/c9nj01380f |
DatabaseName | CrossRef Engineered Materials Abstracts METADEX Technology Research Database Illustrata: Natural Sciences Materials Research Database ProQuest Illustrata: Technology Collection |
DatabaseTitle | CrossRef Materials Research Database ProQuest Illustrata: Natural Sciences Engineered Materials Abstracts ProQuest Illustrata: Technology Collection Technology Research Database METADEX |
DatabaseTitleList | CrossRef Materials Research Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 1369-9261 |
EndPage | 938 |
ExternalDocumentID | 10_1039_C9NJ01380F c9nj01380f |
GroupedDBID | - 0-7 0R 123 1TJ 29N 4.4 70 705 70J 7~J AAEMU AAGNR AAIWI AALRV AANOJ ABDVN ABFLS ABGFH ABPTK ABRYZ ACGFS ACIWK ACLDK ACNCT ADMRA ADSRN AENEX AFVBQ AGKEF AGSTE AGSWI ALMA_UNASSIGNED_HOLDINGS ASKNT AUDPV AZFZN BLAPV BSQNT C6K CKLOX CS3 D0L DU5 DZ EBS ECGLT EE0 EF- EJD F5P GNO HZ H~N IDZ IPNFZ J3I JG L7B M4U N9A O9- OK1 P2P R7B R7C R7D RCNCU RIG RNS RPMJG RRA RRC RSCEA SKA SKF SKH SLH TN5 TWZ VH6 X YNT --- -DZ -~X 0R~ 2WC 70~ AAJAE AAMEH AAWGC AAXHV AAXPP AAYXX ABASK ABCQX ABEMK ABJNI ABPDG ABXOH AEFDR AENGV AESAV AETIL AFLYV AFOGI AFRDS AFRZK AGEGJ AGRSR AHGCF AKMSF ALUYA ANUXI APEMP CITATION GGIMP H13 HZ~ R56 RAOCF YQT 7SR 8BQ 8FD H9R JG9 KA0 |
ID | FETCH-LOGICAL-c307t-80abf75eba5314de4a1f72d72ff2dc6344a816382e4c8010d22cacdda709d5b73 |
ISSN | 1144-0546 |
IngestDate | Mon Jun 30 09:55:52 EDT 2025 Tue Jul 01 00:46:21 EDT 2025 Thu Apr 24 23:06:29 EDT 2025 Sat Jan 08 11:09:32 EST 2022 Wed Nov 11 00:26:55 EST 2020 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 23 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c307t-80abf75eba5314de4a1f72d72ff2dc6344a816382e4c8010d22cacdda709d5b73 |
Notes | Electronic supplementary information (ESI) available. CCDC For ESI and crystallographic data in CIF or other electronic format see DOI 10.1039/c9nj01380f 1058388 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ORCID | 0000-0001-7105-7950 0000-0001-6276-0679 |
PQID | 2237516078 |
PQPubID | 2048886 |
PageCount | 7 |
ParticipantIDs | crossref_citationtrail_10_1039_C9NJ01380F crossref_primary_10_1039_C9NJ01380F rsc_primary_c9nj01380f proquest_journals_2237516078 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 20190610 |
PublicationDateYYYYMMDD | 2019-06-10 |
PublicationDate_xml | – month: 6 year: 2019 text: 20190610 day: 10 |
PublicationDecade | 2010 |
PublicationPlace | Cambridge |
PublicationPlace_xml | – name: Cambridge |
PublicationTitle | New journal of chemistry |
PublicationYear | 2019 |
Publisher | Royal Society of Chemistry |
Publisher_xml | – name: Royal Society of Chemistry |
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 |
SSID | ssj0011761 |
Score | 2.4176986 |
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... |
SourceID | proquest crossref rsc |
SourceType | Aggregation Database Enrichment Source Index Database Publisher |
StartPage | 932 |
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 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3Nb9MwFLe67QAXxNdEx0CW4IImQ5o4Sc2tqjaNaUwcOmnsEjn-aIO6pOraSXDmyv_Mc2wn6VQk4GK1L4lj5f38_LP9_B5CbxkVdEgZdCQY3QmNJfQ5OWBE5JECfj6QrHb5_3yRnF7Ss6v4qtf71fFaWq_y9-LH1nMl_6NVkIFezSnZf9BsUykI4DfoF0rQMJR_peORSQDN58SmZhJH2ntaGWdyGxnWEkxeb8BXUBGR0LA7kM6LqfFpjEZHi1m1qsRsWd34hBnmqK5aloU9VbVSwtNKsGXwapDyG8NO7ziw99suvzXukp1gFMKnk2v4svMAvp5BU74oN2zahWu7B1Twipii8RQq1taPuJySr-t70utZQc4B4NPu4oU5L5UQ58Zq7S3M5wiwRhcN28qihBEW2hjt3kjbWE4OjGHUMbnMrY8q92-4dWAIIhNXVbDym9maDXQ7_DVOie3FHbQXwqwDzObe6Hjy6bzZlhqkNgCvb7WPdxuxD-3TmwynnbbsLH1OmZq7TB6jR27SgUcWQU9QT5VP0YOxV84z9HOEN5CEGyThDpJw_h1zfB9J2CLpI97AEQYR7uAINzjClcYeR7jGEbY4eo4uT44n41Pi8nMQASPDCsgNz3Uaq5yDIadSUT7QaSjTUOtQiiSilA8N3Q8VFUCEAhmGggspeRowGedptI92y6pULxBmUaA5hVoVVzSJJBNpQKUE9pzoNNBxH73z3zQTLni9yaEyz2oniohlY3ZxVn__kz5609y7sCFbtt516FWTuX5xmwFXTmMTcnHYR_ugrub5Vrt9dLD9QraQ-uBPT71ED1v4H6Jd0Jt6BWx2lb92GPsNvRuluw |
linkProvider | Royal Society of Chemistry |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=A+metal-organic+framework+constructed+by+a+viologen-derived+ligand%3A+photochromism+and+discernible+detection+of+volatile+amine+vapors&rft.jtitle=New+journal+of+chemistry&rft.au=Dong%2C+Zhen-Peng&rft.au=Zhao%2C+Jiao-Jiao&rft.au=Liu%2C+Peng-Yu&rft.au=Liu%2C+Zhi-Liang&rft.date=2019-06-10&rft.issn=1144-0546&rft.eissn=1369-9261&rft.volume=43&rft.issue=23&rft.spage=932&rft.epage=938&rft_id=info:doi/10.1039%2Fc9nj01380f&rft.externalDocID=c9nj01380f |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1144-0546&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1144-0546&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1144-0546&client=summon |