TY - JOUR
T1 - Synthesis, characterization, and near-infrared photoluminescence of novel neodymium(III) complexes
AU - He, Hongshan
AU - WONG, Rick W K
AU - Guo, Jianping
AU - Li, King Fai
AU - WONG, Wai Yeung
AU - Lo, Wing Kit
AU - CHEAH, Kok Wai
N1 - Funding Information:
Thanks are due to the Research Grants Council of Hong Kong Special Administrative Region, China (HKBU2023/00P), Hong Kong Baptist University, and Natural Science Foundation of Fujian province, China, for financial support of this work.
PY - 2004
Y1 - 2004
N2 - A series of monoporphyrinate neodymium(III) complexes stabilized by the anionic tripodal ligand hydridotris(pyrazol-1-yl)borate were prepared and characterized. These complexes were characterized by elemental analysis and spectroscopy. The structure of resulting complex was determined by single-crystal X-ray diffraction. The complex crystallized in the monoclinic space group P21, with a 13.7347(11), b 27.156(2), c 15.5397(13) Å, β 114.1490(10)°, and V 5288.8(7)Å3. The neodymium(III) ion is coordinated by four nitrogen atoms from the porphyrinate dianion and three nitrogen atoms from the anionic tripodal ligand. Photoluminescence studies showed that the porphyrinate dianion absorbed light and transferred energy to the Nd3+ centre, a process which then allowed the metal ion to emit efficiently at 885, 900, and 1071 nm. The effects of the substituent and the solvent on emission efficiency were also investigated.
AB - A series of monoporphyrinate neodymium(III) complexes stabilized by the anionic tripodal ligand hydridotris(pyrazol-1-yl)borate were prepared and characterized. These complexes were characterized by elemental analysis and spectroscopy. The structure of resulting complex was determined by single-crystal X-ray diffraction. The complex crystallized in the monoclinic space group P21, with a 13.7347(11), b 27.156(2), c 15.5397(13) Å, β 114.1490(10)°, and V 5288.8(7)Å3. The neodymium(III) ion is coordinated by four nitrogen atoms from the porphyrinate dianion and three nitrogen atoms from the anionic tripodal ligand. Photoluminescence studies showed that the porphyrinate dianion absorbed light and transferred energy to the Nd3+ centre, a process which then allowed the metal ion to emit efficiently at 885, 900, and 1071 nm. The effects of the substituent and the solvent on emission efficiency were also investigated.
UR - http://www.scopus.com/inward/record.url?scp=4444314613&partnerID=8YFLogxK
U2 - 10.1071/CH04005
DO - 10.1071/CH04005
M3 - Journal article
AN - SCOPUS:4444314613
SN - 0004-9425
VL - 57
SP - 803
EP - 810
JO - Australian Journal of Chemistry
JF - Australian Journal of Chemistry
IS - 8
ER -