TY - JOUR
T1 - Solid state dehydration condensation of potassium tetrakis(μ-pyrophosphito-P,P′)diplatinate(II) accompanied by the red shift of the luminescence peak
AU - Yamaguchi, Tadashi
AU - Sasaki, Yoichi
AU - Ikeyama, Takeshi
AU - Azumi, Tohru
AU - Ito, Tasuku
N1 - Funding Information:
University) for the X-ray crystal structure analysis. CP-MAS NMR spectra were measured at JEOL to which authors thanks are due. This work was partly supported by Grant-m-Aid for Scientific Research (No. 01430009) on Priority Area of ‘Dynamic Interactions and Electronic Processes of Macromolecular Complexes’ from the Ministry of Education, Science and Culture, Japan.
PY - 1990/6/15
Y1 - 1990/6/15
N2 - Yellow crystals of K4[Pt2(pop)4]·2H2O (pop2- = pyrophosphite(2-)) change their color to orange upon dehydration in vacuo or at elevated temperatures with concomitant change in the emission color from green (emission peak at 515 nm) to orange (emission peaks at 520, 570, 670 nm). Thermogravimetric, 31P CP-MAS NMR, electronic and infrared absorption spectral studies indicate that the dehydration is not a simple loss of crystalline waters but involves dehydration condensation between the neighboring complex anions. The original green emission is recovered on dissolving the orange solid in water. Emissions from the dehydrated orange solid are of phosphorescence type (τem ≤ 6 μs). Relative intensity of the three emission peaks depends significantly on dehydration conditions, exciting wavelength and temperature. The orange solid seems to contain various species with different extent and type of condensation. Red shift of the emission peak on dehydration was discussed on the basis of the ligand field theory.
AB - Yellow crystals of K4[Pt2(pop)4]·2H2O (pop2- = pyrophosphite(2-)) change their color to orange upon dehydration in vacuo or at elevated temperatures with concomitant change in the emission color from green (emission peak at 515 nm) to orange (emission peaks at 520, 570, 670 nm). Thermogravimetric, 31P CP-MAS NMR, electronic and infrared absorption spectral studies indicate that the dehydration is not a simple loss of crystalline waters but involves dehydration condensation between the neighboring complex anions. The original green emission is recovered on dissolving the orange solid in water. Emissions from the dehydrated orange solid are of phosphorescence type (τem ≤ 6 μs). Relative intensity of the three emission peaks depends significantly on dehydration conditions, exciting wavelength and temperature. The orange solid seems to contain various species with different extent and type of condensation. Red shift of the emission peak on dehydration was discussed on the basis of the ligand field theory.
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U2 - 10.1016/S0020-1693(00)80861-0
DO - 10.1016/S0020-1693(00)80861-0
M3 - Article
AN - SCOPUS:7044226740
SN - 0020-1693
VL - 172
SP - 233
EP - 239
JO - Inorganica Chimica Acta
JF - Inorganica Chimica Acta
IS - 2
ER -