References
- Martinez-Manez, R.; Sancenon, F. Chem. Rev. 2003, 103, 4419. https://doi.org/10.1021/cr010421e
- Suksai, C.; Tuntulani, T. Chem. Soc. Rev. 2003, 32, 192. https://doi.org/10.1039/b209598j
- Beer, P. D.; Gale, P. A. Angew. Chem. Int. Ed. 2001, 40, 486. https://doi.org/10.1002/1521-3773(20010202)40:3<486::AID-ANIE486>3.0.CO;2-P
- Wallington, T. J.; Kaiser, E. W.; Farrell, J. T. Chem. Soc. Rev. 2006, 35, 335. https://doi.org/10.1039/b410469m
- Gale, P. A. Acc. Chem. Res. 2006, 39, 465. https://doi.org/10.1021/ar040237q
- Fabbrizzi, L.; Licchelli, M.; Rabaioli, G.; Taglietti, A. Coord. Chem. Rev. 2000, 205, 85. https://doi.org/10.1016/S0010-8545(00)00239-3
- Niikura, K.; Metzger, A.; Anslyn, E. V. J. Am. Chem. Soc. 1998, 120, 8533. https://doi.org/10.1021/ja980990c
- Aït-Haddou, H.; Wiskur, S. L.; Lynch, V. M.; Anslyn, E. V. J. Am. Chem. Soc. 2001, 123, 11296. https://doi.org/10.1021/ja011905v
- Leung, D.; Folmer-Andersen, J. F.; Lynch, V. M.; Anslyn, E. V. J. Am. Chem. Soc. 2008, 130, 12318. https://doi.org/10.1021/ja803806c
- Folmer-Andersen, J. F.; Lynch, V. M.; Anslyn, E. V. J. Am. Chem. Soc. 2005, 127, 7986. https://doi.org/10.1021/ja052029e
- Vázquez, M.; Fabbrizzi, L.; Taglietti, A.; Pedrido, R. M.; González- Noya, A. M.; Bermejo, M. R. Angew. Chem. Int. Ed. 2004, 43, 1962. https://doi.org/10.1002/anie.200353148
- Lin, Y. S.; Tu, G. M.; Lin, C. Y.; Chang, Y. T.; Yen, Y. P. New. J. Chem. 2009, 33, 860. https://doi.org/10.1039/b811172c
- Kato, R.; Nishizawa, S.; Hayashita, T.; Teramae, N. Tetrahedron Lett. 2001, 42, 5053. https://doi.org/10.1016/S0040-4039(01)00916-9
- Yen, Y. P.; Ho, K. W. Tetrahedron Lett. 2006, 47, 1193. https://doi.org/10.1016/j.tetlet.2005.12.009
- Quinlan, E.; Matthews, S. E.; Gunnlaugsson, T. Tetrahedron Lett. 2006, 47, 9333. https://doi.org/10.1016/j.tetlet.2006.10.112
- Zhou, L. L.; Sun, H.; Li, H. P.; Wang, H.; Zhang, X. H.; Wu, S. K.; Lee, S. T. Org. Lett. 2004, 6, 1071. https://doi.org/10.1021/ol035818e
- Choi, M. K.; Kim, H. N.; Choi, H. J.; Yoon, J.; Hyun, M. H. Tetra hedron Lett. 2008, 49, 4522. https://doi.org/10.1016/j.tetlet.2008.05.055
- Shao, J.; Lin, H.; Lin, H. K. Talanta 2008, 75, 1015. https://doi.org/10.1016/j.talanta.2007.12.041
- Kim, H.-J.; Asif, R.; Chung, D. S.; Hong, J.-I. Tetrahedron Lett. 2003, 44, 4335. https://doi.org/10.1016/S0040-4039(03)00937-7
- Ryu, D.; Park, E.; Kim, D.-S.; Yan, S.; Lee, J. Y.; Chang, B.-Y.; Ahn, K. H. J. Am. Chem. Soc. 2008, 130, 2394. https://doi.org/10.1021/ja078308e
- Kim, H.; So, S. M.; Yen, C. P.; Vinhato, E.; Lough, A. J.; Hong, J.-I.; Kim, H.-J.; Chin, J. Angew. Chem. Int. Ed. 2008, 47, 8657. https://doi.org/10.1002/anie.200803116
- Kral, V.; Andrievsky, A.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 2953. https://doi.org/10.1021/ja00115a041
- Gunnlaugsson, T.; Davis, A. P.; O'Brien, J. E.; Glynn, M. Org. Lett. 2004, 4, 2449.
- Robertson, W. G.; Hughes, H. Scanning Microsc. 1993, 3, 391.
- Liu, S. Y.; Fang, L.; He, Y. B.; Chan, W. H.; Yeung, K. T.; Cheng, Y. K.; Yang, R. H. Org. Lett. 2005, 7, 5825. https://doi.org/10.1021/ol052341t
- Zeng, Z. Y.; He, Y. B.; Wu, J. L.; Wei, L. H.; Liu, X.; Meng, L. Z.; Yang, X. Eur. J. Org. Chem. 2004, 2888.
- Raker, J.; Glass, T. E. J. Org. Chem. 2002, 67, 6113. https://doi.org/10.1021/jo025903k
- Linton, B. R.; Goodman, M. S.; Fan, E.; Arman, S. A.; Hamilton, A. D. J. Org. Chem. 2001, 66, 7313. https://doi.org/10.1021/jo010413y
- Ghosh, K.; Saha, I.; Masanta, G.; Wang, E. B.; Parish, C. A. Tetrahedron Lett. 2010, 51, 343. https://doi.org/10.1016/j.tetlet.2009.11.021
- Ghosh, K.; Masanta, G.; Chattopadhyay, A. P. Eur. J. Org. Chem. 2009, 4515.
- Singh, N.; Lee, G. W.; Jang, D. O. Tetrahedron 2008, 64, 1482. https://doi.org/10.1016/j.tet.2007.11.040
- Moriuchi, T.; Yoshida, K.; Hirao, T. Org. Lett. 2003, 5, 4285. https://doi.org/10.1021/ol030098x
- Ghosh, K.; Masanta, G. Tetrahedron Lett. 2008, 49, 2592. https://doi.org/10.1016/j.tetlet.2008.02.095
- Goswami, S.; Dey, S.; Jana, S. Tetrahedron 2008, 64, 6358. https://doi.org/10.1016/j.tet.2008.04.086
- Tang, L. J.; Park, J.; Kim, H. J.; Kim, Y.; Kim, S. J.; Chin, J.; Kim, K. M. J. Am. Chem. Soc. 2008, 130, 12606. https://doi.org/10.1021/ja804753n
- Fabbrizzi, L.; Licchelli, M.; Mancin, F.; Pizzeghello, M.; Rabaioli, G.; Taglietti, A.; Tecilla, P.; Tonellato, U. Chem. Eur. J. 2001, 7, 94. https://doi.org/10.1002/1521-3765(20010105)7:1<94::AID-CHEM94>3.0.CO;2-M
- Wiskur, S. L.; Ait-Haddou, H.; Lavigne, J. J.; Anslyn, E. V. Acc. Chem. Res. 2001, 34, 963. https://doi.org/10.1021/ar9600796
- Wright, A. T.; Anslyn, E. V. Chem. Soc. Rev. 2006, 35, 14. https://doi.org/10.1039/b505518k
- Zhu, L.; Zhong, Z. L.; Anslyn, E. V. J. Am. Chem. Soc. 2005, 127, 4260. https://doi.org/10.1021/ja0435945
- Nguyen, B. T.; Anslyn, E. V. Coord. Chem. Rev. 2006, 250, 3118. https://doi.org/10.1016/j.ccr.2006.04.009
- Boiocchi, M.; Bonizzoni, M.; Fabbrizzi, L.; Piovani, G.; Taglietti, A. Angew. Chem. Int. Ed. 2004, 43, 3847. https://doi.org/10.1002/anie.200460036
- Boiocchi, M.; Bonizzoni, M.; Moletti, A.; Pasini, D.; Taglietti, A. New. J. Chem. 2007, 31, 352. https://doi.org/10.1039/b616492g
- Lee, J. H.; Park, J.; Lah, M. S.; Chin, J.; Hong, J.-I. Org. Lett. 2007, 9, 3729. https://doi.org/10.1021/ol071306e
- Tang, L. J.; Li, Y.; Zhang, H.; Guo, Z. L.; Qian, J. H. Tetrahedron Lett. 2009, 50, 6844. https://doi.org/10.1016/j.tetlet.2009.09.133
- Schmuck, C.; Bickert, V.; Merschky, M.; Geiger, L.; Rupprecht, D.; Dudaczek, J.; Wich, P.; Rehm, T.; Machon, U. Eur. J. Org. Chem. 2008, 324.
- Schmuck, C. Chem. Eur. J. 2000, 6, 709. https://doi.org/10.1002/(SICI)1521-3765(20000218)6:4<709::AID-CHEM709>3.0.CO;2-6
- Connors, K. A. Binding Constants-the Measurement of Molecular Complex Stability; John Wiley & Sons: New York, USA, 1987.
- Kim, S. Y.; Hong, J.-I. Tetrahedron Lett. 2009, 50, 1951. https://doi.org/10.1016/j.tetlet.2009.02.036
Cited by
- Highly selective and sensitive fluorescent sensing of oxalate in water vol.48, pp.55, 2012, https://doi.org/10.1039/c2cc33191h
- ) complexes of macrocyclic and open-chain pseudopeptidic ligands: synthesis, characterization and interaction with dicarboxylates vol.44, pp.28, 2015, https://doi.org/10.1039/C5DT01496D
- Selective recognition of oxalate in water: effect of pH on binding strength and sensing mechanisms vol.53, pp.82, 2017, https://doi.org/10.1039/C7CC06955C
- complex pp.15227235, 2017, https://doi.org/10.1002/bio.3410
- Fluorescent Recognition of Pyrophosphate in Water by a New Chemosensing ensemble vol.35, pp.8, 2010, https://doi.org/10.3184/174751911x13129777578197
- Colorimetric Recognition of Oxalate in Water by a New Carbazole-Zn(II) Based Chemosensing Ensemble vol.37, pp.9, 2010, https://doi.org/10.3184/174751913x13738775726772
- Recyclable chemosensor for oxalate based on bimetallic complexes of a dinucleating bis(iminopyridine) ligand vol.43, pp.21, 2010, https://doi.org/10.1039/c4dt00577e
- Development of a New Colorimetric Chemosensor for Selective Determination of Urinary and Vegetable Oxalate Concentration Through an Indicator Displacement Assay (IDA) in Aqueous Media vol.56, pp.3, 2010, https://doi.org/10.17113/ftb.56.03.18.5726
- A Simple Paper-based Colorimetric Device for Rapid and Sensitive Urinary Oxalate Determinations vol.34, pp.1, 2018, https://doi.org/10.2116/analsci.34.103