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Enrique J. Baran Evelina G. Ferrer Maria C. Apella 《Monatshefte für Chemie / Chemical Monthly》1991,122(1-2):21-26
Summary Electronic and vibrational spectra of bis(imidazol)copper(II)diacetate were investigated in order to obtain a wider insight into the structural properties of this interesting complex compound, which presents high cytotoxic activity. Electronic transitions were investigated by reflectance measurements of the solid and by absorption, using aqueous and methanolic solutions. IR spectra could be interpreted on the basis of the characteristic ligand vibrations. Some information could also be obtained for the Cu-N and Cu-O vibrations. For comparative purposes, the IR spectrum of Cu(imidazol)4I2 was also recorded and analyzed. 相似文献
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Chen D Albuquerque IF Baublis VV Bondar NF Carrigan RA Cooper PS Lisheng D Denisov AS Dobrovolsky AV Dubbs T Endler AM Escobar CO Foucher M Golovtsov VL Goritchev PA Gottschalk H Gouffon P Grachev VT Khanzadeev AV Kubantsev MA Kuropatkin NP Lach J Lang Pengfei Lebedenko VN Li Chengze Li Yunshan Mahon JR McCliment E Morelos A Newsom C Pommot Maia MC Samsonov VM Schegelsky VA Shi Huanzhang Smith VJ Sun CR Tang Fukun Terentyev NK Timm S Tkatch II Uvarov LN Vorobyov AA Yan Jie Zhao Wenheng 《Physical review letters》1992,69(23):3286-3289
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Foucher M Albuquerque IF Bondar NF Carrigan R Chen D Li Chengze Cooper PS Denisov AS Dobrovolsky AV Dubbs T Endler AM Escobar CO Tang Fukun Golovtsov VL Goritchev PA Gottschalk H Gouffon P Grachev VT Shi Huanzhang Yan Jie Khanzadeev AV Kubantsev MA Kuropatkin NP Lach J Luksys M Lebedenko VN Dai Lisheng Mahon JR McCliment E Morelos A Newsom C Lang Pengfei Pommot Maia MC Samsonov VM Zheng Shuchen Smith VJ Terentyev NK Timm S Tkatch II Uvarov LN Vorobyov AA Zhao Wenheng Zhong Yuanyuan 《Physical review letters》1992,68(20):3004-3007
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García Rodenas L Palacios JM Apella MC Morando PJ Blesa MA 《Journal of colloid and interface science》2005,290(1):145-154
Electrophoretic mobilities of various synthetic and semisynthetic hydroxyapatites (Ca10(PO4)6(OH)2, HAP) suspended in aqueous solutions have been measured as a function of pH and calcium concentration. The studied powders differ in particle size, crystallinity degree and surface contamination (carbonate). When equilibrated in mineral acids or bases, a large plateau of negative mobility is observed in the pH range 5-8, with increasing negative values at higher pH. Only in the case of the sample composed of nanoparticles, positive mobility obtains at pH < 8.9. When Ca2+ is added, positive mobility values are observed for all samples, and a bell-shaped profile results as a function of pH. Two possible models are explored to describe the results: the Nernstian approach, which assumes solubility equilibrium and surface potentials determined by the three potential-determining ions (Ca2+, PO3-4, and OH-), and the surface complexation approach, based on the idea of negligible phase transfer of structural phosphate. The Nernstian model is inadequate, whereas a very simple surface complexation model based on the equations Ca5(PO4)+3 = Ca4(PO4)-3 + Ca2+,Ca4(PO4)-3 + H+ = Ca4(PO4)2(PO4H),Ca5(PO4)+3 + OH- = Ca5(PO4)3(OH),coupled with a very simple electrical double layer, model suffices to reproduce the bell-shaped profile of the mobility as a function of pH in the presence of added calcium salts. The results also show that the sample composed of nanoparticles exchanges ions more easily with the solution, without reaching the solubility equilibrium in the explored timespans. In the presence of soluble phosphate salts, it is postulated that the same surface ensembles define the surface charge, with participation of phosphate as described by the equation Ca5(PO4)+3 + PO3-4 = Ca4(PO4)-3.HAP is just one member of a family of calcium phosphates with different (Ca)/(P) ratios. Electrophoretic mobilities of another member, tricalcium diphosphate, Ca3(PO4)2, were also measured and shown to be described by the same basic model. Comparison with previous literature data shows that the negative plateau in the mobility is a general feature of many HAP samples at low Ca2+, again in agreement with the surface complexation model. FTIR data demonstrates that surface phosphate indeed undergoes protonation, as postulated in the model. 相似文献