Synthesis of endohedral $^{133}$ Xe-fullerenol by using higher fullerene

Watanabe, Satoshi; Katabuchi, Tatsuya*; Ishioka, Noriko; Matsuhashi, Shimpei

Hydrophilic endohedral $^{133}$ Xe-fullerenols [ $^{133}$ Xe@C $_{76}$ (OH) $_{x}$ and $^{133}$ Xe@C $_{84}$ (OH) $_{x}$ ] were synthesized from hydrophobic endohedral $^{133}$ Xe-fullerenes. The yields were found to depend on the solubility of endohedral $^{133}$ Xe-fullerenols in o-dichlorobenzene and water phases, reflecting the number of OH groups of the product. The endohedral $^{133}$ Xe-fullerenols stored in 0.9 % NaCl solution were stable enough for the use in nuclear medicine.

Language	:	English
Journal	:	Journal of Nuclear and Radiochemical Sciences
Volume	:	8
Number	:	2
Pages	:	p.105 - 107
Publication Year/Month	:	2007/10
Meeting title	:	6th International Symposium on Advanced Science Research; Frontiers of Nuclear and Radiochemistry (ASR 2006)
Held date	:	2006/10
Location (city)	:	Tokai
Location (country)	:	Japan
Patent information	:
PDF	:
Paper URL	:	https://doi.org/10.14494/jnrs2000.8.105
DOI for research data	:
Keywords	:	no keyword
Research Facility	:	TIARA(イオン照射研究施設)
Press Release	:
Article of JAEA R&D Review	:
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Registration No. : BB20071789
JAEA Abstracts No. : 36000174
Paper Submission No. : 3504

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Synthesis of endohedral Xe-fullerenol by using higher fullerene

Synthesis of endohedral $^{133}$ Xe-fullerenol by using higher fullerene