Facile Synthesis of Isomerically Pure Fullerenols and Formation of Spherical Aggregates from C60(OH)8

被引:63
作者
Zhang, Gang [3 ]
Liu, Yun [1 ]
Liang, Dehai [1 ]
Gan, Liangbing [2 ,3 ]
Li, Yuliang [3 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Minist Educ, Key Lab Polymer Chem & Phys, Beijing 100871, Peoples R China
[2] Peking Univ, Coll Chem & Mol Engn, Minist Educ, Key Lab Bioorgan Chem & Mol Engn, Beijing 100871, Peoples R China
[3] Chinese Acad Sci, Inst Chem, CAS Key Lab Organ Solids, Beijing Natl Lab Mol Sci, Beijing 100080, Peoples R China
关键词
fullerenes; alcohols; self-assembly; synthetic methods; WATER-SOLUBLE FULLERENES; EFFICIENT SYNTHESIS; MIXED PEROXIDES; IN-VITRO; C-60; HYDROPEROXIDE; DERIVATIVES; CHEMISTRY; VESICLES; LIGHT;
D O I
10.1002/anie.201001280
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Octahydroxy fullerene C60(OH)8 (see picture) is among the isomerically pure fullerenols with two to eight OH groups that were prepared by selective transformation of fert-butylperoxo groups of fullerene mixed peroxides. Since C60(OH)8 has all OH groups on the same hemisphere, it is amphiphilic and forms stable spherical aggregates in water. (Figure Presented) © 2010 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:5293 / 5295
页数:3
相关论文
共 23 条
[1]   Fullerenol-Cytotoxic Conjugates for Cancer Chemotherapy [J].
Chaudhuri, Padmaparna ;
Paraskar, Abhimanyu ;
Soni, Shivani ;
Mashelkar, Raghunath A. ;
Sengupta, Shiladitya .
ACS NANO, 2009, 3 (09) :2505-2514
[2]   EVIDENCE OF HEMIKETALS INCORPORATED IN THE STRUCTURE OF FULLEROLS DERIVED FROM AQUEOUS ACID CHEMISTRY [J].
CHIANG, LY ;
UPASANI, RB ;
SWIRCZEWSKI, JW ;
SOLED, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (13) :5453-5457
[3]   MULTIHYDROXY ADDITIONS ONTO C-60 FULLERENE MOLECULES [J].
CHIANG, LY ;
SWIRCZEWSKI, JW ;
HSU, CS ;
CHOWDHURY, SK ;
CAMERON, S ;
CREEGAN, K .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (24) :1791-1793
[4]   FREE-RADICAL SCAVENGING ACTIVITY OF WATER-SOLUBLE FULLERENOLS [J].
CHIANG, LY ;
LU, FJ ;
LIN, JT .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (12) :1283-1284
[5]   VERSATILE NITRONIUM CHEMISTRY FOR C-60 FULLERENE FUNCTIONALIZATION [J].
CHIANG, LY ;
UPASANI, RB ;
SWIRCZEWSKI, JW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (26) :10154-10157
[6]   EFFICIENT SYNTHESIS OF POLYHYDROXYLATED FULLERENE DERIVATIVES VIA HYDROLYSIS OF POLYCYCLOSULFATED PRECURSORS [J].
CHIANG, LY ;
WANG, LY ;
SWIRCZEWSKI, JW ;
SOLED, S ;
CAMERON, S .
JOURNAL OF ORGANIC CHEMISTRY, 1994, 59 (14) :3960-3968
[7]   Fullerenes as a tert-butylperoxy radical trap, metal catalyzed reaction of tert-butyl hydroperoxide with fullerenes, and formation of the first fullerene mixed peroxides C60(O)(OOtBu)4 and C70(OOtBu)10 [J].
Gan, LB ;
Huang, SH ;
Zhang, XA ;
Zhang, AX ;
Cheng, BC ;
Cheng, H ;
Li, XL ;
Shang, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (45) :13384-13385
[8]   Synthesis and in vitro characterization of a tissue-selective fullerene:: Vectoring C60(OH)16AMBP to mineralized bone [J].
Gonzalez, KA ;
Wilson, LJ ;
Wu, WJ ;
Nancollas, GH .
BIOORGANIC & MEDICINAL CHEMISTRY, 2002, 10 (06) :1991-1997
[9]   Activity of water-soluble fullerenes towards •OH-radicals and molecular oxygen [J].
Guldi, DM ;
Asmus, KD .
RADIATION PHYSICS AND CHEMISTRY, 1999, 56 (04) :449-456
[10]  
Homma T., 2010, ANGEW CHEM, V122, P1709