User menu

A coumarin-based "turn-on" fluorescent sensor for the determination of Al3+: single crystal X-ray structure and cell staining properties

Bibliographic reference Guha, Subarna ; Lohar, Sisir ; Sahana , Animesh ; Banerje, Arnab ; Safin, Damir ; et. al. A coumarin-based "turn-on" fluorescent sensor for the determination of Al3+: single crystal X-ray structure and cell staining properties. In: Dalton Transactions, Vol. 42, p. 10198-10207 (2013)
Permanent URL
  1. Delhaize, Plant Physiol., 107, 315 (1995)
  2. Crapper McLachlan D. R., Lukiw W. J., Kruck T. P. A., Aluminum, altered transcription, and the pathogenesis of Alzheimer's disease, 10.1007/bf01734059
  3. Valeur B, Design principles of fluorescent molecular sensors for cation recognition, 10.1016/s0010-8545(00)00246-0
  4. Flaten Trond Peder, Aluminium as a risk factor in Alzheimer’s disease, with emphasis on drinking water, 10.1016/s0361-9230(01)00459-2
  5. R. Walton Judie, Evidence that Ingested Aluminum Additives Contained in Processed Foods and Alum-Treated Drinking Water are a Major Risk Factor for Alzheimers Disease, 10.2174/1877944111202010019
  6. Woodson G.C., An Interesting Case of Osteomalacia Due to Antacid Use Associated With Stainable Bone Aluminum in a Patient With Normal Renal Function, 10.1016/s8756-3282(98)00060-x
  7. Darbre P.D., Aluminium, antiperspirants and breast cancer, 10.1016/j.jinorgbio.2005.06.001
  8. Fasman Gerald D., Aluminum and Alzheimer's disease: model studies, 10.1016/s0010-8545(96)90020-x
  9. Sargazi Mansour, Roberts Norman B, Shenkin Alan, In-vitro studies of aluminium-induced toxicity on kidney proximal tubular cells, 10.1016/s0162-0134(01)00312-9
  10. Yousef Mokhtar I., El-Morsy Ahmed M.A., Hassan Mervat S., Aluminium-induced deterioration in reproductive performance and seminal plasma biochemistry of male rabbits: Protective role of ascorbic acid, 10.1016/j.tox.2005.06.025
  11. Soni Madhusudan G., White Susan M., Flamm W.Gary, Burdock George A., Safety Evaluation of Dietary Aluminum, 10.1006/rtph.2000.1441
  12. Baylor Norman W., Egan William, Richman Paul, Aluminum salts in vaccines—US perspective, 10.1016/s0264-410x(02)00166-4
  13. Exley Christopher, Guest editorial, 10.1016/j.jinorgbio.2005.07.004
  14. Soroka Krystyna., Vithanage Rathnapala S., Phillips Denise A., Walker Brian., Dasgupta Purnendu K., Fluorescence properties of metal complexes of 8-hydroxyquinoline-5-sulfonic acid and chromatographic applications, 10.1021/ac00131a019
  15. Launay Franck, Alain Vale′rie, Destandau Émilie, Ramos Nathalie, Bardez Ēlisabeth, Baret Paul, Pierre Jean-Louis, From 8-hydroxy-5-sulfoquinoline to new related fluorogenic ligands for complexation of aluminium(III) and gallium(III), 10.1039/b103406p
  16. Bakker Eric, Bühlmann Philippe, Pretsch Ernö, Carrier-Based Ion-Selective Electrodes and Bulk Optodes. 1. General Characteristics, 10.1021/cr940394a
  17. Salmon Lionel, Thuéry Pierre, Rivière Eric, Ephritikhine Michel, Synthesis, Structure, and Magnetic Behavior of a Series of Trinuclear Schiff Base Complexes of 5f (UIV, ThIV) and 3d (CuII, ZnII) Ions, 10.1021/ic0512375
  18. da Silveira Vivian Chagas, Luz Juliana Silva, Oliveira Carla Columbano, Graziani Ilaria, Ciriolo Maria Rosa, Ferreira Ana Maria da Costa, Double-strand DNA cleavage induced by oxindole-Schiff base copper(II) complexes with potential antitumor activity, 10.1016/j.jinorgbio.2007.12.033
  19. Padhyé Subhash, Kauffman George B., Transition metal complexes of semicarbazones and thiosemicarbazones, 10.1016/0010-8545(85)80022-9
  20. Kasselouri Spyridoula, Garoufis Achilleas, Katehanakis Agathopous, Kalkanis George, Perlepes Spyros P., Hadjiliadis Nick, 1:1 Metal complexes of 2-(2′-pyridyl)quinoxaline, a ligand unexpectedly formed by the reaction between 2-acetylpyridine and 1,2-phenylenediamine, 10.1016/s0020-1693(00)90718-7
  21. Cano-pavón J.M., Trujillo M.L., García De Torres A., 3-Hydroxypyridine-2-aldehyde 2-pyridylhydrazone as an analytical reagent, 10.1016/0003-2670(80)87032-2
  22. Jiang C, Spectrofluorimetric determination of trace amounts of aluminium with 5-bromo-salicylaldehyde salicyloylhydrazone, 10.1016/s0039-9140(96)02033-4
  23. Maity Debabrata, Govindaraju T., A differentially selective sensor with fluorescence turn-on response to Zn2+and dual-mode ratiometric response to Al3+in aqueous media, 10.1039/c1cc16064h
  24. Maity Debabrata, Govindaraju T., Naphthaldehyde-Urea/Thiourea Conjugates as Turn-On Fluorescent Probes for Al3+ Based on Restricted C=N Isomerization, 10.1002/ejic.201100772
  25. de Pablos Fernando, Ariza Jos� Luis G�mez, Pino Francisco, N-oxalylamine(salicylaldehyde hydrazone) as an analytical fluorimetric reagent for the determination of nanogram amounts of aluminium, 10.1039/an9861101159
  26. Karak Debasis, Lohar Sisir, Sahana Animesh, Guha Subarna, Banerjee Arnab, Das Debasis, An Al3+ induced green luminescent fluorescent probe for cell imaging and naked eye detection, 10.1039/c2ay25226k
  27. Mánuel-Vez M, Fluorimetric determination traces of aluminium in soil extracts, 10.1016/0039-9140(94)e0072-y
  28. Briggs Mark S.J, Fossey John S, Richards Christopher J, Scott Brian, Whateley John, Towards novel biolabels: synthesis of a tagged highly fluorescent Schiff-base aluminium complex, 10.1016/s0040-4039(02)00953-x
  29. Arduini Maria, Felluga Fulvia, Mancin Fabrizio, Rossi Paola, Tecilla Paolo, Tonellato Umberto, Valentinuzzi Nicola, Aluminium fluorescence detection with a FRET amplified chemosensorElectronic supplementary information (ESI) available: experimental details and spectra. See, 10.1039/b303195k
  30. Maity Debabrata, Govindaraju T., Pyrrolidine constrained bipyridyl-dansyl click fluoroionophore as selective Al3+sensor, 10.1039/c0cc00119h
  31. Othman Amel Ben, Lee Jeong Won, Huh Young-Duk, Abidi Rym, Kim Jong Seung, Vicens Jacques, A novel pyrenyl-appended tricalix[4]arene for fluorescence-sensing of Al(III), 10.1016/j.tet.2007.06.120
  32. Wang Yan-Wei, Yu Meng-Xiao, Yu Yan-Hong, Bai Zhi-Ping, Shen Zhen, Li Fu-You, You Xiao-Zeng, A colorimetric and fluorescent turn-on chemosensor for Al3+ and its application in bioimaging, 10.1016/j.tetlet.2009.08.078
  33. Sai Sathish R., Goutam Raju A., Nageswara Rao G., Janardhana C., A fluorescent fluoride ion probe based on a self-organized ensemble of 5-hydroxyflavone–Al(III) complex, 10.1016/j.saa.2007.04.018
  34. Zhao Yonggang, Lin Zhihua, Liao Haiping, Duan Chunying, Meng Qingjin, A highly selective fluorescent chemosensor for Al3+ derivated from 8-hydroxyquinoline, 10.1016/j.inoche.2006.05.030
  35. Jeanson Aurélie, Béreau Virginie, Fluorescence detection of Al(III) using derivatives of oxazoline and imidazoline, 10.1016/j.inoche.2005.09.034
  36. Maity Debabrata, Govindaraju T., Conformationally Constrained (Coumarin−Triazolyl−Bipyridyl) Click Fluoroionophore as a Selective Al3+Sensor, 10.1021/ic1009994
  37. Lu Yan, Huang Shanshan, Liu Yiyang, He Song, Zhao Liancheng, Zeng Xianshun, Highly Selective and Sensitive Fluorescent Turn-on Chemosensor for Al3+Based on a Novel Photoinduced Electron Transfer Approach, 10.1021/ol202054v
  38. Sahana Animesh, Banerjee Arnab, Das Sudipta, Lohar Sisir, Karak Debasis, Sarkar Bidisha, Kanti Mukhopadhyay Subhra, Mukherjee Asok K., Das Debasis, A naphthalene-based Al3+ selective fluorescent sensor for living cell imaging, 10.1039/c1ob05479a
  39. Wang Lina, Qin Wenwu, Tang Xiaoliang, Dou Wei, Liu Weisheng, Teng Qingfeng, Yao Xiaojun, A selective, cell-permeable fluorescent probe for Al3+ in living cells, 10.1039/c0ob00123f
  40. Gou Chao, Qin Shao-Hui, Wu Hai-Qiang, Wang Yu, Luo Jing, Liu Xiao-Ya, A highly selective chemosensor for Cu2+ and Al3+ in two different ways based on Salicylaldehyde Schiff, 10.1016/j.inoche.2011.06.024
  41. Oliveira Elisabete, Santos Hugo M., Capelo José Luis, Lodeiro Carlos, New emissive dopamine derivatives as fluorescent chemosensors for metal ions: A CHEF effect for Al(III) interaction, 10.1016/j.ica.2011.08.033
  42. Jiang Xin-hui, Wang Bao-dui, Yang Zheng-yin, Liu Yong-chun, Li Tian-rong, Liu Zeng-chen, 8-Hydroxyquinoline-5-carbaldehyde Schiff-base as a highly selective and sensitive Al3+ sensor in weak acid aqueous medium, 10.1016/j.inoche.2011.04.027
  43. Banerjee Arnab, Sahana Animesh, Das Sudipta, Lohar Sisir, Guha Subarna, Sarkar Bidisha, Mukhopadhyay Subhra Kanti, Mukherjee Asok K., Das Debasis, A naphthalene exciplex based Al3+ selective on-type fluorescent probe for living cells at the physiological pH range: experimental and computational studies, 10.1039/c2an16233d
  44. Das Sudipta, Sahana Animesh, Banerjee Arnab, Lohar Sisir, Safin Damir A., Babashkina Maria G., Bolte Michael, Garcia Yann, Hauli Ipsit, Mukhopadhyay Subhra Kanti, Das Debasis, Ratiometric fluorescence sensing and intracellular imaging of Al3+ ions driven by an intramolecular excimer formation of a pyrimidine–pyrene scaffold, 10.1039/c3dt32908a
  45. te Velde G., Bickelhaupt F. M., Baerends E. J., Fonseca Guerra C., van Gisbergen S. J. A., Snijders J. G., Ziegler T., Chemistry with ADF, 10.1002/jcc.1056
  46. Mitoraj Mariusz P., Michalak Artur, Ziegler Tom, A Combined Charge and Energy Decomposition Scheme for Bond Analysis, 10.1021/ct800503d
  47. de Silva A. Prasanna, Moody Thomas S., Wright Glenn D., Fluorescent PET (Photoinduced Electron Transfer) sensors as potent analytical tools, 10.1039/b912527m
  48. SASAMOT Kazumi, USHIJIMA Tamano, SAITO Mikihiko, OHKURA Yosuke, Precolumn Fluorescence Derivatization of Carboxylic Acids Using 4-Aminomethyl-6,7-dimethoxycoumarin in a Two-Phase Medium., 10.2116/analsci.12.189
  49. Maliakal Ashok, Lem George, Turro Nicholas J., Ravichandran Ravi, Suhadolnik Joseph C., DeBellis Anthony D., Wood Mervin G., Lau Jacqueline, Twisted Intramolecular Charge Transfer States in 2-Arylbenzotriazoles:  Fluorescence Deactivation via Intramolecular Electron Transfer Rather Than Proton Transfer, 10.1021/jp021000j
  50. Benesi H. A., Hildebrand J. H., A Spectrophotometric Investigation of the Interaction of Iodine with Aromatic Hydrocarbons, 10.1021/ja01176a030
  51. Parr Robert G., Pearson Ralph G., Absolute hardness: companion parameter to absolute electronegativity, 10.1021/ja00364a005
  52. Ziegler Tom, Rauk Arvi, On the calculation of bonding energies by the Hartree Fock Slater method : I. The transition state method, 10.1007/bf02401406
  53. Guha Subarna, Lohar Sisir, Bolte Michael, Safin Damir A., Das Debasis, Crystal Structure and Interaction of 6-Amino Coumarin with Nitrite Ion for Its Selective Fluorescence Detection, 10.1080/00387010.2011.605416
  55. Spek Anthony L., Structure validation in chemical crystallography, 10.1107/s090744490804362x
  56. Sheldrick George M., A short history ofSHELX, 10.1107/s0108767307043930
  57. Bruno Ian J., Cole Jason C., Edgington Paul R., Kessler Magnus, Macrae Clare F., McCabe Patrick, Pearson Jonathan, Taylor Robin, New software for searching the Cambridge Structural Database and visualizing crystal structures, 10.1107/s0108768102003324