Water-stable Cd()/Zn() coordination polymers as recyclable luminescent sensors for detecting hippuric acid in simulated urine for indexing toluene exposure with high selectivity, sensitivity and fast response

Three novel Cd( ii )/Zn( ii ) coordination polymers (CPs), namely [Cd(L)(BPDC) 0.5 H 2 O]·0.5H 2 O ( 1 ), [Zn 2 (L) 2 (BPDC)]·2H 2 O ( 2 ) and [Cd 2 (L)(BTC)H 2 O]·3H 2 O ( 3 ) (L = 4-(tetrazol-5-yl)phenyl-4,2′:6′,4′′-terpyridine, H 2 BPDC = 4,4′-biphenyldicarboxylic acid, and H 3 BTC = 1,3,5-benzen...

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Published inDalton transactions : an international journal of inorganic chemistry Vol. 5; no. 2; pp. 553 - 561
Main Authors Zhao, Jiao-Jiao, Zhang, Lei, Liu, Peng-Yu, Chen, Wei-Zhe, Liu, Zhi-Liang, Wang, Yan-Qin
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 14.01.2021
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Abstract Three novel Cd( ii )/Zn( ii ) coordination polymers (CPs), namely [Cd(L)(BPDC) 0.5 H 2 O]·0.5H 2 O ( 1 ), [Zn 2 (L) 2 (BPDC)]·2H 2 O ( 2 ) and [Cd 2 (L)(BTC)H 2 O]·3H 2 O ( 3 ) (L = 4-(tetrazol-5-yl)phenyl-4,2′:6′,4′′-terpyridine, H 2 BPDC = 4,4′-biphenyldicarboxylic acid, and H 3 BTC = 1,3,5-benzenetricarboxylic acid), have been successfully synthesized and characterized. CP 1 and CP 2 display new two-dimensional double-layered honeycomb frameworks containing uncoordinated nitrogen atoms from pyridine and tetrazole rings, which can easily form hydrogen bonds with various analytes. CP 3 exhibits a 3D framework also with uncoordinated nitrogen atoms from pyridine and tetrazole rings. The fluorescence explorations indicate that CPs 1-3 exhibit strong blue luminescence and excellent chemical stability under a relatively wide range of pH conditions. It is worth noting that CPs 1-3 can quantitatively detect hippuric acid (HA), which is a metabolite of toluene in human urine, with high selectivity, sensitivity, fast response and relatively low detection limits. Moreover, the sensing mechanism of CPs 1-3 for HA can mainly be ascribed to fluorescence resonance energy transfer (FRET). CPs 1-3 could be ideal candidates as HA sensors in human urine samples for practical applications. Notably, to the best of our knowledge, we report for the first time Cd( ii )/Zn( ii )-based luminescent sensors for detecting HA in simulated urine. Water stable Cd( ii )/Zn( ii ) coordination polymers exhibit rapid, sensitive, selective and recyclable detection towards hippuric acid in simulated urine for indexing toluene exposure.
AbstractList Three novel Cd(ii)/Zn(ii) coordination polymers (CPs), namely [Cd(L)(BPDC)0.5H2O]·0.5H2O (1), [Zn2(L)2(BPDC)]·2H2O (2) and [Cd2(L)(BTC)H2O]·3H2O (3) (L = 4-(tetrazol-5-yl)phenyl-4,2':6',4''-terpyridine, H2BPDC = 4,4'-biphenyldicarboxylic acid, and H3BTC = 1,3,5-benzenetricarboxylic acid), have been successfully synthesized and characterized. CP 1 and CP 2 display new two-dimensional double-layered honeycomb frameworks containing uncoordinated nitrogen atoms from pyridine and tetrazole rings, which can easily form hydrogen bonds with various analytes. CP 3 exhibits a 3D framework also with uncoordinated nitrogen atoms from pyridine and tetrazole rings. The fluorescence explorations indicate that CPs 1-3 exhibit strong blue luminescence and excellent chemical stability under a relatively wide range of pH conditions. It is worth noting that CPs 1-3 can quantitatively detect hippuric acid (HA), which is a metabolite of toluene in human urine, with high selectivity, sensitivity, fast response and relatively low detection limits. Moreover, the sensing mechanism of CPs 1-3 for HA can mainly be ascribed to fluorescence resonance energy transfer (FRET). CPs 1-3 could be ideal candidates as HA sensors in human urine samples for practical applications. Notably, to the best of our knowledge, we report for the first time Cd(ii)/Zn(ii)-based luminescent sensors for detecting HA in simulated urine.Three novel Cd(ii)/Zn(ii) coordination polymers (CPs), namely [Cd(L)(BPDC)0.5H2O]·0.5H2O (1), [Zn2(L)2(BPDC)]·2H2O (2) and [Cd2(L)(BTC)H2O]·3H2O (3) (L = 4-(tetrazol-5-yl)phenyl-4,2':6',4''-terpyridine, H2BPDC = 4,4'-biphenyldicarboxylic acid, and H3BTC = 1,3,5-benzenetricarboxylic acid), have been successfully synthesized and characterized. CP 1 and CP 2 display new two-dimensional double-layered honeycomb frameworks containing uncoordinated nitrogen atoms from pyridine and tetrazole rings, which can easily form hydrogen bonds with various analytes. CP 3 exhibits a 3D framework also with uncoordinated nitrogen atoms from pyridine and tetrazole rings. The fluorescence explorations indicate that CPs 1-3 exhibit strong blue luminescence and excellent chemical stability under a relatively wide range of pH conditions. It is worth noting that CPs 1-3 can quantitatively detect hippuric acid (HA), which is a metabolite of toluene in human urine, with high selectivity, sensitivity, fast response and relatively low detection limits. Moreover, the sensing mechanism of CPs 1-3 for HA can mainly be ascribed to fluorescence resonance energy transfer (FRET). CPs 1-3 could be ideal candidates as HA sensors in human urine samples for practical applications. Notably, to the best of our knowledge, we report for the first time Cd(ii)/Zn(ii)-based luminescent sensors for detecting HA in simulated urine.
Three novel Cd( ii )/Zn( ii ) coordination polymers (CPs), namely [Cd(L)(BPDC) 0.5 H 2 O]·0.5H 2 O ( 1 ), [Zn 2 (L) 2 (BPDC)]·2H 2 O ( 2 ) and [Cd 2 (L)(BTC)H 2 O]·3H 2 O ( 3 ) (L = 4-(tetrazol-5-yl)phenyl-4,2′:6′,4′′-terpyridine, H 2 BPDC = 4,4′-biphenyldicarboxylic acid, and H 3 BTC = 1,3,5-benzenetricarboxylic acid), have been successfully synthesized and characterized. CP 1 and CP 2 display new two-dimensional double-layered honeycomb frameworks containing uncoordinated nitrogen atoms from pyridine and tetrazole rings, which can easily form hydrogen bonds with various analytes. CP 3 exhibits a 3D framework also with uncoordinated nitrogen atoms from pyridine and tetrazole rings. The fluorescence explorations indicate that CPs 1–3 exhibit strong blue luminescence and excellent chemical stability under a relatively wide range of pH conditions. It is worth noting that CPs 1–3 can quantitatively detect hippuric acid (HA), which is a metabolite of toluene in human urine, with high selectivity, sensitivity, fast response and relatively low detection limits. Moreover, the sensing mechanism of CPs 1–3 for HA can mainly be ascribed to fluorescence resonance energy transfer (FRET). CPs 1–3 could be ideal candidates as HA sensors in human urine samples for practical applications. Notably, to the best of our knowledge, we report for the first time Cd( ii )/Zn( ii )-based luminescent sensors for detecting HA in simulated urine.
Three novel Cd( ii )/Zn( ii ) coordination polymers (CPs), namely [Cd(L)(BPDC) 0.5 H 2 O]·0.5H 2 O ( 1 ), [Zn 2 (L) 2 (BPDC)]·2H 2 O ( 2 ) and [Cd 2 (L)(BTC)H 2 O]·3H 2 O ( 3 ) (L = 4-(tetrazol-5-yl)phenyl-4,2′:6′,4′′-terpyridine, H 2 BPDC = 4,4′-biphenyldicarboxylic acid, and H 3 BTC = 1,3,5-benzenetricarboxylic acid), have been successfully synthesized and characterized. CP 1 and CP 2 display new two-dimensional double-layered honeycomb frameworks containing uncoordinated nitrogen atoms from pyridine and tetrazole rings, which can easily form hydrogen bonds with various analytes. CP 3 exhibits a 3D framework also with uncoordinated nitrogen atoms from pyridine and tetrazole rings. The fluorescence explorations indicate that CPs 1-3 exhibit strong blue luminescence and excellent chemical stability under a relatively wide range of pH conditions. It is worth noting that CPs 1-3 can quantitatively detect hippuric acid (HA), which is a metabolite of toluene in human urine, with high selectivity, sensitivity, fast response and relatively low detection limits. Moreover, the sensing mechanism of CPs 1-3 for HA can mainly be ascribed to fluorescence resonance energy transfer (FRET). CPs 1-3 could be ideal candidates as HA sensors in human urine samples for practical applications. Notably, to the best of our knowledge, we report for the first time Cd( ii )/Zn( ii )-based luminescent sensors for detecting HA in simulated urine. Water stable Cd( ii )/Zn( ii ) coordination polymers exhibit rapid, sensitive, selective and recyclable detection towards hippuric acid in simulated urine for indexing toluene exposure.
Three novel Cd(ii)/Zn(ii) coordination polymers (CPs), namely [Cd(L)(BPDC) H O]·0.5H O (1), [Zn (L) (BPDC)]·2H O (2) and [Cd (L)(BTC)H O]·3H O (3) (L = 4-(tetrazol-5-yl)phenyl-4,2':6',4''-terpyridine, H BPDC = 4,4'-biphenyldicarboxylic acid, and H BTC = 1,3,5-benzenetricarboxylic acid), have been successfully synthesized and characterized. CP 1 and CP 2 display new two-dimensional double-layered honeycomb frameworks containing uncoordinated nitrogen atoms from pyridine and tetrazole rings, which can easily form hydrogen bonds with various analytes. CP 3 exhibits a 3D framework also with uncoordinated nitrogen atoms from pyridine and tetrazole rings. The fluorescence explorations indicate that CPs 1-3 exhibit strong blue luminescence and excellent chemical stability under a relatively wide range of pH conditions. It is worth noting that CPs 1-3 can quantitatively detect hippuric acid (HA), which is a metabolite of toluene in human urine, with high selectivity, sensitivity, fast response and relatively low detection limits. Moreover, the sensing mechanism of CPs 1-3 for HA can mainly be ascribed to fluorescence resonance energy transfer (FRET). CPs 1-3 could be ideal candidates as HA sensors in human urine samples for practical applications. Notably, to the best of our knowledge, we report for the first time Cd(ii)/Zn(ii)-based luminescent sensors for detecting HA in simulated urine.
Three novel Cd(ii)/Zn(ii) coordination polymers (CPs), namely [Cd(L)(BPDC)0.5H2O]·0.5H2O (1), [Zn2(L)2(BPDC)]·2H2O (2) and [Cd2(L)(BTC)H2O]·3H2O (3) (L = 4-(tetrazol-5-yl)phenyl-4,2′:6′,4′′-terpyridine, H2BPDC = 4,4′-biphenyldicarboxylic acid, and H3BTC = 1,3,5-benzenetricarboxylic acid), have been successfully synthesized and characterized. CP 1 and CP 2 display new two-dimensional double-layered honeycomb frameworks containing uncoordinated nitrogen atoms from pyridine and tetrazole rings, which can easily form hydrogen bonds with various analytes. CP 3 exhibits a 3D framework also with uncoordinated nitrogen atoms from pyridine and tetrazole rings. The fluorescence explorations indicate that CPs 1–3 exhibit strong blue luminescence and excellent chemical stability under a relatively wide range of pH conditions. It is worth noting that CPs 1–3 can quantitatively detect hippuric acid (HA), which is a metabolite of toluene in human urine, with high selectivity, sensitivity, fast response and relatively low detection limits. Moreover, the sensing mechanism of CPs 1–3 for HA can mainly be ascribed to fluorescence resonance energy transfer (FRET). CPs 1–3 could be ideal candidates as HA sensors in human urine samples for practical applications. Notably, to the best of our knowledge, we report for the first time Cd(ii)/Zn(ii)-based luminescent sensors for detecting HA in simulated urine.
Author Zhao, Jiao-Jiao
Liu, Peng-Yu
Liu, Zhi-Liang
Zhang, Lei
Wang, Yan-Qin
Chen, Wei-Zhe
AuthorAffiliation Inner Mongolia Key Laboratory of Chemistry and Physics of Rare Earth Materials
Inner Mongolia University
College of Chemistry and Chemical Engineering
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Cites_doi 10.1021/acs.accounts.7b00387
10.1016/0892-0362(88)90014-1
10.1016/j.snb.2017.07.020
10.1080/15321810600734901
10.1021/jacs.6b01663
10.1016/j.snb.2017.12.060
10.1021/ic9019553
10.1002/(SICI)1099-0801(199803/04)12:2<47::AID-BMC717>3.0.CO;2-Y
10.1039/b802426j
10.1039/C6TC05615F
10.1021/ja500090y
10.1039/D0TC00825G
10.1021/jacs.6b09463
10.1039/C5CC02596F
10.1016/j.ccr.2011.03.013
10.1039/C9QI01490J
10.1039/C6TA05965A
10.1021/cg3000526
10.1039/C9TB02579K
10.1039/C8CS00688A
10.1002/adfm.201707169
10.1016/j.jchromb.2010.12.015
10.1289/ehp.99107417
10.1039/C4CS00010B
10.1080/00958972.2016.1143935
10.1039/b807083k
10.1021/acssensors.7b00808
10.1039/C6CE01457G
10.1093/jat/31.6.347
10.1016/j.arabjc.2010.09.029
10.1021/acsami.6b14795
10.1039/c2cs35047e
10.1021/acs.cgd.6b00258
10.1016/j.ccr.2011.02.012
10.1039/D0CS00107D
10.1016/S0378-4347(00)00463-1
10.1039/C5CC05219J
10.1039/C6CE01035K
10.1016/j.legalmed.2005.02.001
10.1021/jacs.0c05074
10.3390/s141018886
10.1021/jacs.5b06929
10.1021/cg050458i
10.1002/anie.200902274
10.1016/j.jpba.2010.01.016
10.1002/anie.201812708
10.1039/C7TB01764B
10.1039/C5PP00107B
10.1038/s41467-019-11912-4
10.1016/j.aca.2017.11.039
10.1038/s41560-017-0018-7
10.1021/cg0604982
10.1021/acs.cgd.6b00528
10.1039/C8NJ05647A
10.1080/00039896.1992.9935940
10.1016/j.bios.2016.12.026
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References Wang (D0DT03648J-(cit46)/*[position()=1]) 2019; 10
Afreen (D0DT03648J-(cit32)/*[position()=1]) 2020; 8
Erucar (D0DT03648J-(cit25)/*[position()=1]) 2017; 5
Wang (D0DT03648J-(cit42)/*[position()=1]) 2016; 138
Yoshida (D0DT03648J-(cit57)/*[position()=1]) 2005; 7
Hu (D0DT03648J-(cit26)/*[position()=1]) 2014; 43
Hao (D0DT03648J-(cit5)/*[position()=1]) 2015; 51
Inagaki (D0DT03648J-(cit12)/*[position()=1]) 2006; 27
Yang (D0DT03648J-(cit45)/*[position()=1]) 2017; 2
Gao (D0DT03648J-(cit24)/*[position()=1]) 2017; 9
Pan (D0DT03648J-(cit15)/*[position()=1]) 2011; 255
Kim (D0DT03648J-(cit33)/*[position()=1]) 2020; 49
Feldman (D0DT03648J-(cit3)/*[position()=1]) 1999; 107
Wang (D0DT03648J-(cit50)/*[position()=1]) 2016; 18
Penner (D0DT03648J-(cit13)/*[position()=1]) 2010; 52
Zhang (D0DT03648J-(cit52)/*[position()=1]) 2010; 49
Wang (D0DT03648J-(cit39)/*[position()=1]) 2019; 58
Zhong (D0DT03648J-(cit29)/*[position()=1]) 2020; 7
Chen (D0DT03648J-(cit56)/*[position()=1]) 2017; 5
Guo (D0DT03648J-(cit41)/*[position()=1]) 2019; 43
Otto (D0DT03648J-(cit4)/*[position()=1]) 1992; 47
Kirchon (D0DT03648J-(cit16)/*[position()=1]) 2018; 47
Wen (D0DT03648J-(cit48)/*[position()=1]) 2007; 7
Wang (D0DT03648J-(cit40)/*[position()=1]) 2016; 18
Falkowski (D0DT03648J-(cit23)/*[position()=1]) 2014; 136
Yan (D0DT03648J-(cit17)/*[position()=1]) 2017; 50
Liu (D0DT03648J-(cit54)/*[position()=1]) 2015; 14
Choi (D0DT03648J-(cit58)/*[position()=1]) 2014; 14
Li (D0DT03648J-(cit38)/*[position()=1]) 2016; 16
Niu (D0DT03648J-(cit49)/*[position()=1]) 2012; 12
Wen (D0DT03648J-(cit51)/*[position()=1]) 2006; 6
Zhang (D0DT03648J-(cit31)/*[position()=1]) 2015; 137
Kim (D0DT03648J-(cit18)/*[position()=1]) 2018; 3
Wu (D0DT03648J-(cit27)/*[position()=1]) 2018; 28
Li (D0DT03648J-(cit37)/*[position()=1]) 2016; 16
Lv (D0DT03648J-(cit43)/*[position()=1]) 2017; 139
Wang (D0DT03648J-(cit14)/*[position()=1]) 2009; 48
Li (D0DT03648J-(cit19)/*[position()=1]) 2009; 38
He (D0DT03648J-(cit44)/*[position()=1]) 2020; 142
Ellairaja (D0DT03648J-(cit59)/*[position()=1]) 2017; 91
Park (D0DT03648J-(cit6)/*[position()=1]) 2007; 31
Qin (D0DT03648J-(cit9)/*[position()=1]) 2017; 253
Du (D0DT03648J-(cit1)/*[position()=1]) 2018; 1001
Qin (D0DT03648J-(cit47)/*[position()=1]) 2018; 259
Wu (D0DT03648J-(cit28)/*[position()=1]) 2020; 8
Zhao (D0DT03648J-(cit8)/*[position()=1]) 2011; 879
Wu (D0DT03648J-(cit30)/*[position()=1]) 2018; 28
Xu (D0DT03648J-(cit55)/*[position()=1]) 2015; 51
Rosenberg (D0DT03648J-(cit2)/*[position()=1]) 1988; 10
Zinalibdin (D0DT03648J-(cit7)/*[position()=1]) 2013; 6
Li (D0DT03648J-(cit20)/*[position()=1]) 2011; 255
Kongtip (D0DT03648J-(cit10)/*[position()=1]) 2001; 751
Ma (D0DT03648J-(cit21)/*[position()=1]) 2009; 38
Sheldrick (D0DT03648J-(cit34)/*[position()=1]) 1996
Yang (D0DT03648J-(cit11)/*[position()=1]) 1998; 12
Lia (D0DT03648J-(cit36)/*[position()=1]) 2016; 69
Lv (D0DT03648J-(cit53)/*[position()=1]) 2016; 4
Dhakshinamoorthy (D0DT03648J-(cit22)/*[position()=1]) 2012; 41
References_xml – issn: 1996
  publication-title: Program for Empirical Absorption Correction of Area Detector Data
  doi: Sheldrick
– issn: 1998
  publication-title: SHELXTL Version 5.1
  doi: Sheldrick
– volume: 50
  start-page: 2789
  year: 2017
  ident: D0DT03648J-(cit17)/*[position()=1]
  publication-title: Acc. Chem. Res.
  doi: 10.1021/acs.accounts.7b00387
– volume: 10
  start-page: 489
  year: 1988
  ident: D0DT03648J-(cit2)/*[position()=1]
  publication-title: Neurotoxicol. Teratol.
  doi: 10.1016/0892-0362(88)90014-1
– volume: 253
  start-page: 852
  year: 2017
  ident: D0DT03648J-(cit9)/*[position()=1]
  publication-title: Sens. Actuators, B
  doi: 10.1016/j.snb.2017.07.020
– volume-title: Program for Empirical Absorption Correction of Area Detector Data
  year: 1996
  ident: D0DT03648J-(cit34)/*[position()=1]
– volume: 27
  start-page: 213
  year: 2006
  ident: D0DT03648J-(cit12)/*[position()=1]
  publication-title: J. Immunoassay Immunochem.
  doi: 10.1080/15321810600734901
– volume: 138
  start-page: 6204
  year: 2016
  ident: D0DT03648J-(cit42)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b01663
– volume: 259
  start-page: 125
  year: 2018
  ident: D0DT03648J-(cit47)/*[position()=1]
  publication-title: Sens. Actuators, B
  doi: 10.1016/j.snb.2017.12.060
– volume: 49
  start-page: 1535
  year: 2010
  ident: D0DT03648J-(cit52)/*[position()=1]
  publication-title: Inorg. Chem.
  doi: 10.1021/ic9019553
– volume: 12
  start-page: 47
  year: 1998
  ident: D0DT03648J-(cit11)/*[position()=1]
  publication-title: Biomed. Chromatogr.
  doi: 10.1002/(SICI)1099-0801(199803/04)12:2<47::AID-BMC717>3.0.CO;2-Y
– volume: 38
  start-page: 1477
  year: 2009
  ident: D0DT03648J-(cit19)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/b802426j
– volume: 5
  start-page: 2015
  year: 2017
  ident: D0DT03648J-(cit56)/*[position()=1]
  publication-title: J. Mater. Chem. C
  doi: 10.1039/C6TC05615F
– volume: 136
  start-page: 5213
  year: 2014
  ident: D0DT03648J-(cit23)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja500090y
– volume: 8
  start-page: 6820
  year: 2020
  ident: D0DT03648J-(cit28)/*[position()=1]
  publication-title: J. Mater. Chem. C
  doi: 10.1039/D0TC00825G
– volume: 139
  start-page: 211
  year: 2017
  ident: D0DT03648J-(cit43)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b09463
– volume: 51
  start-page: 10280
  year: 2015
  ident: D0DT03648J-(cit55)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C5CC02596F
– volume: 255
  start-page: 1921
  year: 2011
  ident: D0DT03648J-(cit15)/*[position()=1]
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/j.ccr.2011.03.013
– volume: 7
  start-page: 1161
  year: 2020
  ident: D0DT03648J-(cit29)/*[position()=1]
  publication-title: Inorg. Chem. Front.
  doi: 10.1039/C9QI01490J
– volume: 4
  start-page: 15494
  year: 2016
  ident: D0DT03648J-(cit53)/*[position()=1]
  publication-title: J. Mater. Chem. A
  doi: 10.1039/C6TA05965A
– volume: 12
  start-page: 2397
  year: 2012
  ident: D0DT03648J-(cit49)/*[position()=1]
  publication-title: Cryst. Growth Des.
  doi: 10.1021/cg3000526
– volume: 8
  start-page: 1338
  year: 2020
  ident: D0DT03648J-(cit32)/*[position()=1]
  publication-title: J. Mater. Chem. B
  doi: 10.1039/C9TB02579K
– volume: 47
  start-page: 8611
  year: 2018
  ident: D0DT03648J-(cit16)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C8CS00688A
– volume: 28
  start-page: 1707169
  year: 2018
  ident: D0DT03648J-(cit30)/*[position()=1]
  publication-title: Adv. Funct. Mater.
  doi: 10.1002/adfm.201707169
– volume: 879
  start-page: 296
  year: 2011
  ident: D0DT03648J-(cit8)/*[position()=1]
  publication-title: J. Chromatogr. B: Anal. Technol. Biomed. Life Sci.
  doi: 10.1016/j.jchromb.2010.12.015
– volume: 107
  start-page: 417
  year: 1999
  ident: D0DT03648J-(cit3)/*[position()=1]
  publication-title: Environ. Health Perspect.
  doi: 10.1289/ehp.99107417
– volume: 43
  start-page: 5815
  year: 2014
  ident: D0DT03648J-(cit26)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C4CS00010B
– volume: 69
  start-page: 966
  year: 2016
  ident: D0DT03648J-(cit36)/*[position()=1]
  publication-title: J. Coord. Chem.
  doi: 10.1080/00958972.2016.1143935
– volume: 38
  start-page: 1248
  year: 2009
  ident: D0DT03648J-(cit21)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/b807083k
– volume: 3
  start-page: 386
  year: 2018
  ident: D0DT03648J-(cit18)/*[position()=1]
  publication-title: ACS Sens.
  doi: 10.1021/acssensors.7b00808
– volume: 18
  start-page: 7471
  year: 2016
  ident: D0DT03648J-(cit50)/*[position()=1]
  publication-title: CrystEngComm
  doi: 10.1039/C6CE01457G
– volume: 31
  start-page: 347
  year: 2007
  ident: D0DT03648J-(cit6)/*[position()=1]
  publication-title: J. Anal. Toxicol.
  doi: 10.1093/jat/31.6.347
– volume: 28
  start-page: 1707169
  year: 2018
  ident: D0DT03648J-(cit27)/*[position()=1]
  publication-title: Adv. Funct. Mater.
  doi: 10.1002/adfm.201707169
– volume: 6
  start-page: 115
  year: 2013
  ident: D0DT03648J-(cit7)/*[position()=1]
  publication-title: Arabian J. Chem.
  doi: 10.1016/j.arabjc.2010.09.029
– volume: 9
  start-page: 3455
  year: 2017
  ident: D0DT03648J-(cit24)/*[position()=1]
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.6b14795
– volume: 41
  start-page: 5262
  year: 2012
  ident: D0DT03648J-(cit22)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c2cs35047e
– volume: 16
  start-page: 2912
  year: 2016
  ident: D0DT03648J-(cit37)/*[position()=1]
  publication-title: Cryst. Growth Des.
  doi: 10.1021/acs.cgd.6b00258
– volume: 255
  start-page: 1791
  year: 2011
  ident: D0DT03648J-(cit20)/*[position()=1]
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/j.ccr.2011.02.012
– volume: 49
  start-page: 5446
  year: 2020
  ident: D0DT03648J-(cit33)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/D0CS00107D
– volume: 751
  start-page: 199
  year: 2001
  ident: D0DT03648J-(cit10)/*[position()=1]
  publication-title: J. Chromatogr. B: Biomed. Sci. Appl.
  doi: 10.1016/S0378-4347(00)00463-1
– volume: 51
  start-page: 14509
  year: 2015
  ident: D0DT03648J-(cit5)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C5CC05219J
– volume: 18
  start-page: 5101
  year: 2016
  ident: D0DT03648J-(cit40)/*[position()=1]
  publication-title: CrystEngComm
  doi: 10.1039/C6CE01035K
– volume: 7
  start-page: 198
  year: 2005
  ident: D0DT03648J-(cit57)/*[position()=1]
  publication-title: Leg. Med.
  doi: 10.1016/j.legalmed.2005.02.001
– volume: 142
  start-page: 13491
  year: 2020
  ident: D0DT03648J-(cit44)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.0c05074
– volume: 14
  start-page: 18886
  year: 2014
  ident: D0DT03648J-(cit58)/*[position()=1]
  publication-title: Sensors
  doi: 10.3390/s141018886
– volume: 137
  start-page: 12203
  year: 2015
  ident: D0DT03648J-(cit31)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.5b06929
– volume: 6
  start-page: 530
  year: 2006
  ident: D0DT03648J-(cit51)/*[position()=1]
  publication-title: Cryst. Growth Des.
  doi: 10.1021/cg050458i
– volume: 48
  start-page: 5291
  year: 2009
  ident: D0DT03648J-(cit14)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200902274
– volume: 52
  start-page: 534
  year: 2010
  ident: D0DT03648J-(cit13)/*[position()=1]
  publication-title: J. Pharm. Biomed. Anal.
  doi: 10.1016/j.jpba.2010.01.016
– volume: 58
  start-page: 3481
  year: 2019
  ident: D0DT03648J-(cit39)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201812708
– volume: 5
  start-page: 7342
  year: 2017
  ident: D0DT03648J-(cit25)/*[position()=1]
  publication-title: J. Mater. Chem. B
  doi: 10.1039/C7TB01764B
– volume: 14
  start-page: 1644
  year: 2015
  ident: D0DT03648J-(cit54)/*[position()=1]
  publication-title: Photochem. Photobiol. Sci.
  doi: 10.1039/C5PP00107B
– volume: 10
  start-page: 3861
  year: 2019
  ident: D0DT03648J-(cit46)/*[position()=1]
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-019-11912-4
– volume: 1001
  start-page: 134
  year: 2018
  ident: D0DT03648J-(cit1)/*[position()=1]
  publication-title: Anal. Chim. Acta
  doi: 10.1016/j.aca.2017.11.039
– volume: 2
  start-page: 877
  year: 2017
  ident: D0DT03648J-(cit45)/*[position()=1]
  publication-title: Nat. Energy
  doi: 10.1038/s41560-017-0018-7
– volume: 7
  start-page: 93
  year: 2007
  ident: D0DT03648J-(cit48)/*[position()=1]
  publication-title: Cryst. Growth Des.
  doi: 10.1021/cg0604982
– volume: 16
  start-page: 3969
  year: 2016
  ident: D0DT03648J-(cit38)/*[position()=1]
  publication-title: Cryst. Growth Des.
  doi: 10.1021/acs.cgd.6b00528
– volume: 43
  start-page: 2353
  year: 2019
  ident: D0DT03648J-(cit41)/*[position()=1]
  publication-title: New J. Chem.
  doi: 10.1039/C8NJ05647A
– volume: 47
  start-page: 23
  year: 1992
  ident: D0DT03648J-(cit4)/*[position()=1]
  publication-title: Arch. Environ. Health
  doi: 10.1080/00039896.1992.9935940
– volume: 91
  start-page: 82
  year: 2017
  ident: D0DT03648J-(cit59)/*[position()=1]
  publication-title: Biosens. Bioelectron.
  doi: 10.1016/j.bios.2016.12.026
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Snippet Three novel Cd( ii )/Zn( ii ) coordination polymers (CPs), namely [Cd(L)(BPDC) 0.5 H 2 O]·0.5H 2 O ( 1 ), [Zn 2 (L) 2 (BPDC)]·2H 2 O ( 2 ) and [Cd 2 (L)(BTC)H...
Three novel Cd(ii)/Zn(ii) coordination polymers (CPs), namely [Cd(L)(BPDC) H O]·0.5H O (1), [Zn (L) (BPDC)]·2H O (2) and [Cd (L)(BTC)H O]·3H O (3) (L =...
Three novel Cd(ii)/Zn(ii) coordination polymers (CPs), namely [Cd(L)(BPDC)0.5H2O]·0.5H2O (1), [Zn2(L)2(BPDC)]·2H2O (2) and [Cd2(L)(BTC)H2O]·3H2O (3) (L =...
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SubjectTerms Acids
Cadmium
Cadmium - chemistry
Cadmium - urine
Coordination Complexes - chemical synthesis
Coordination Complexes - chemistry
Coordination polymers
Crystallography
Energy transfer
Fluorescence
Hippurates - chemistry
Hippurates - urine
Hippuric acid
Humans
Hydrogen bonds
Limit of Detection
Metabolites
Nitrogen atoms
Polymers - chemistry
Selectivity
Sensitivity
Sensors
Tetrazoles
Toluene
Toluene - chemistry
Urine
Water - chemistry
Zinc - chemistry
Zinc - urine
Title Water-stable Cd()/Zn() coordination polymers as recyclable luminescent sensors for detecting hippuric acid in simulated urine for indexing toluene exposure with high selectivity, sensitivity and fast response
URI https://www.ncbi.nlm.nih.gov/pubmed/33350995
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