Research output: Contribution to journal › Article › peer-review
Halochromic coordination polymers based on a triarylmethane dye for reversible detection of acids. / Zavakhina, Marina S.; Yushina, Irina V.; Samsonenko, Denis G. et al.
In: Dalton Transactions, Vol. 46, No. 2, 01.01.2017, p. 465-470.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Halochromic coordination polymers based on a triarylmethane dye for reversible detection of acids
AU - Zavakhina, Marina S.
AU - Yushina, Irina V.
AU - Samsonenko, Denis G.
AU - Dybtsev, Danil N.
AU - Fedin, Vladimir P.
AU - Argent, Stephen P.
AU - Blake, Alexander J.
AU - Schröder, Martin
PY - 2017/1/1
Y1 - 2017/1/1
N2 - Chromeazurol B (Na2HL) is a pH-sensitive (halochromic) dye based on a hydroxytriarylmethane core and two carboxylate functional groups, which makes it suitable for the synthesis of coordination polymers. Two new coordination polymers [NaZn4(H2O)3(L)3]·3THF·3H2O (1) and [Zn3(H2O)3(μ2-OH2)(μ3-OH)(HL)2(H2L)]·2THF·3H2O (2) incorporating Chromeazurol B linkers have been prepared and characterised. The structure of 1 comprises pentanuclear heterometallic {Zn4Na} nodes linked by six L3− anions to give a layered structure with a honeycomb topology. 2 crystallizes as a double-chain ribbon (ladder) structure with two types of metal node: a mononuclear Zn(ii) cation and tetranuclear {Zn(ii)}4 cluster. Chromeazurol B anions link each tetranuclear cluster to four individual Zn(ii) cations and each Zn(ii) cation with four tetranuclear clusters. Both compounds show pH-sensitivity in water solution which can be observed visually, giving the first example of a halochromic coordination polymer. The halochromic properties of 1 towards HCl vapors were systematically investigated. As-synthesized violet-grey 1 reversibly changes color from orange to pink in the presence of vapors of 2 M and 7 M HCl, respectively. The coordination of the Chromeazurol B anion at each color stage was examined by diffuse reflectance spectroscopy and FT-IR measurements. The remarkable stability of 1 to acid and the observed reversible and reproducible color changes provide a new design for multifunctional sensor materials.
AB - Chromeazurol B (Na2HL) is a pH-sensitive (halochromic) dye based on a hydroxytriarylmethane core and two carboxylate functional groups, which makes it suitable for the synthesis of coordination polymers. Two new coordination polymers [NaZn4(H2O)3(L)3]·3THF·3H2O (1) and [Zn3(H2O)3(μ2-OH2)(μ3-OH)(HL)2(H2L)]·2THF·3H2O (2) incorporating Chromeazurol B linkers have been prepared and characterised. The structure of 1 comprises pentanuclear heterometallic {Zn4Na} nodes linked by six L3− anions to give a layered structure with a honeycomb topology. 2 crystallizes as a double-chain ribbon (ladder) structure with two types of metal node: a mononuclear Zn(ii) cation and tetranuclear {Zn(ii)}4 cluster. Chromeazurol B anions link each tetranuclear cluster to four individual Zn(ii) cations and each Zn(ii) cation with four tetranuclear clusters. Both compounds show pH-sensitivity in water solution which can be observed visually, giving the first example of a halochromic coordination polymer. The halochromic properties of 1 towards HCl vapors were systematically investigated. As-synthesized violet-grey 1 reversibly changes color from orange to pink in the presence of vapors of 2 M and 7 M HCl, respectively. The coordination of the Chromeazurol B anion at each color stage was examined by diffuse reflectance spectroscopy and FT-IR measurements. The remarkable stability of 1 to acid and the observed reversible and reproducible color changes provide a new design for multifunctional sensor materials.
KW - ADSORPTION
KW - CAPTURE
KW - CONSTRUCTION
KW - FLUORESCENT PH SENSOR
KW - HYDROGEN
KW - IONS
KW - LIGAND
KW - METAL-ORGANIC FRAMEWORKS
KW - MOF
KW - SPIN-CROSSOVER
UR - http://www.scopus.com/inward/record.url?scp=85008479958&partnerID=8YFLogxK
U2 - 10.1039/c6dt03969c
DO - 10.1039/c6dt03969c
M3 - Article
C2 - 27957580
AN - SCOPUS:85008479958
VL - 46
SP - 465
EP - 470
JO - Dalton Transactions
JF - Dalton Transactions
SN - 1477-9226
IS - 2
ER -
ID: 10316849