Balancing the acidity of the pendant urea arm of bis-heteroleptic ruthenium(ii) complex containing pyridyl triazole for improved oxyanion recognitionElectronic supplementary information (ESI) available: Experimental section, calculation of binding constants and extraction efficiency, spectral characterization of each compound, solution state 1H NMR studies, ITC experiments, photophysical studies with complex 1[PF6]2/2[PF6]2 and anions, extraction studies. See DOI: 10.1039/c8dt01023d

Balancing the acidity of the pendant urea arm of bis-heteroleptic ruthenium(ii) complex... Two new RuII-based bis-heteroleptic ditopic receptors 1[PF6]2 (C44H34F12N10OP2Ru) and 2[PF6]2 (C40H27F17N10OP2Ru), decorated with a 1-naphthyl and pentafluorophenyl urea pendant arm, respectively, along with the previously reported 3[PF6]2 (C40H31F13N10OP2Ru), containing a pendant 4-fluorophenyl urea unit and 4[PF6]2, devoid of a pendant urea arm, have been studied to establish the role of urea proton acidity on the sensing and extraction of oxyanions in the presence of triazole CH as an additional hydrogen bonding motif. 1H-NMR, isothermal titration calorimetry (ITC) and photophysical experiments show selective binding of 1[PF6]2 and 2[PF6]2 toward oxyanions such as phosphates (e.g., H2PO4 and HP2O73) and carboxylates (e.g., CH3CO2 and PhCO2) like 3[PF6]2. This generalizes the role of triazole CH and urea in the RuII-based bis-heteroleptic ditopic receptors towards recognition of such anions. Interestingly, complex 1[PF6]2 having intermediate acidic urea NH protons showed the highest binding affinity with phosphates as compared to the other urea analogues 2[PF6]2 and 3[PF6]2 as well as the non-urea analogue, 4[PF6]2 (C32H24F12N8P2Ru). Moreover, 2[PF6]2 having the most acidic NH protons showed higher binding affinity towards carboxylates as compared to that of 1[PF6]2/3[PF6]2. Detailed photo-physical studies revealed that 1[PF6]2 is a farsuperior and more selective H2PO4 sensor compared to 2[PF6]2/3[PF6]2/4[PF6]2, as evidenced by the higher degree of amplification of RuII center-based MLCT emission, greater change in excited state lifetime, lower detection limit and higher degree of selectivity. Furthermore, 1[PF6]2 also acts as a moderate liquidliquid extraction agent of H2PO4, CH3CO2 and PhCO2 anions, which was comparable to 3[PF6]2 and much higher as compared to 2[PF6]2/4[PF6]2. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Dalton Transactions Royal Society of Chemistry

Balancing the acidity of the pendant urea arm of bis-heteroleptic ruthenium(ii) complex containing pyridyl triazole for improved oxyanion recognitionElectronic supplementary information (ESI) available: Experimental section, calculation of binding constants and extraction efficiency, spectral characterization of each compound, solution state 1H NMR studies, ITC experiments, photophysical studies with complex 1[PF6]2/2[PF6]2 and anions, extraction studies. See DOI: 10.1039/c8dt01023d

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Publisher
The Royal Society of Chemistry
Copyright
This journal is © The Royal Society of Chemistry
ISSN
1477-9226
eISSN
1477-9234
D.O.I.
10.1039/c8dt01023d
Publisher site
See Article on Publisher Site

Abstract

Two new RuII-based bis-heteroleptic ditopic receptors 1[PF6]2 (C44H34F12N10OP2Ru) and 2[PF6]2 (C40H27F17N10OP2Ru), decorated with a 1-naphthyl and pentafluorophenyl urea pendant arm, respectively, along with the previously reported 3[PF6]2 (C40H31F13N10OP2Ru), containing a pendant 4-fluorophenyl urea unit and 4[PF6]2, devoid of a pendant urea arm, have been studied to establish the role of urea proton acidity on the sensing and extraction of oxyanions in the presence of triazole CH as an additional hydrogen bonding motif. 1H-NMR, isothermal titration calorimetry (ITC) and photophysical experiments show selective binding of 1[PF6]2 and 2[PF6]2 toward oxyanions such as phosphates (e.g., H2PO4 and HP2O73) and carboxylates (e.g., CH3CO2 and PhCO2) like 3[PF6]2. This generalizes the role of triazole CH and urea in the RuII-based bis-heteroleptic ditopic receptors towards recognition of such anions. Interestingly, complex 1[PF6]2 having intermediate acidic urea NH protons showed the highest binding affinity with phosphates as compared to the other urea analogues 2[PF6]2 and 3[PF6]2 as well as the non-urea analogue, 4[PF6]2 (C32H24F12N8P2Ru). Moreover, 2[PF6]2 having the most acidic NH protons showed higher binding affinity towards carboxylates as compared to that of 1[PF6]2/3[PF6]2. Detailed photo-physical studies revealed that 1[PF6]2 is a farsuperior and more selective H2PO4 sensor compared to 2[PF6]2/3[PF6]2/4[PF6]2, as evidenced by the higher degree of amplification of RuII center-based MLCT emission, greater change in excited state lifetime, lower detection limit and higher degree of selectivity. Furthermore, 1[PF6]2 also acts as a moderate liquidliquid extraction agent of H2PO4, CH3CO2 and PhCO2 anions, which was comparable to 3[PF6]2 and much higher as compared to 2[PF6]2/4[PF6]2.

Journal

Dalton TransactionsRoyal Society of Chemistry

Published: May 23, 2018

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