2015
DOI: 10.1155/2015/567073
|View full text |Cite
|
Sign up to set email alerts
|

Review of Synthesis and Antioxidant Potential of Fullerenol Nanoparticles

Abstract: This review describes the chemical synthesis of polar polyhydroxylated fullerene C60derivatives, fullerenols C60(OH)n,2≤n≤44, C60HzOx(OH)y, and polyanion fullerenols C60(OH)15(ONa)9, ranging from the very first synthetic methods up to some contemporary approaches to synthesis and separation. It also provides some basic information about physical characteristics of fullerenols. With the increasing number of hydroxyl groups, water solubility of fullerenols increases as well. Fullerenols both in water and biologi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
56
0
1

Year Published

2016
2016
2021
2021

Publication Types

Select...
8
2

Relationship

1
9

Authors

Journals

citations
Cited by 81 publications
(62 citation statements)
references
References 72 publications
0
56
0
1
Order By: Relevance
“…In this context the halogenation of fullerenes (with fluorine, chlorine, or bromine) is one of the most common chemical reactions to yield derivatives that can be either used as they are or serve as precursors in substitution reactions to sequentially attach aromatic groups to the fullerene cage [17][18][19][20]. In the case of brominated fullerene the substitution of the bromine with OH groups results in derivatives with better solubility in water and in aqueous solutions [21,22]. Polyhydroxylated fullerene or fullerols (C 60 (OH) n ), have attracted much scientific and industrial attention in engineering [23][24][25], where they were found to improve the corrosion resistance and microhardness of coatings [23], to give better mechanical properties than C 60 , when incorporated in poly(styrene-co-4-vinylpyridine), in catalysis [26][27][28], for optical limiting performance [24] or to reinforce and have antioxidation effects when mixed with natural rubber to inhibit the decrease of tensile strength after aging [25].…”
Section: Introductionmentioning
confidence: 99%
“…In this context the halogenation of fullerenes (with fluorine, chlorine, or bromine) is one of the most common chemical reactions to yield derivatives that can be either used as they are or serve as precursors in substitution reactions to sequentially attach aromatic groups to the fullerene cage [17][18][19][20]. In the case of brominated fullerene the substitution of the bromine with OH groups results in derivatives with better solubility in water and in aqueous solutions [21,22]. Polyhydroxylated fullerene or fullerols (C 60 (OH) n ), have attracted much scientific and industrial attention in engineering [23][24][25], where they were found to improve the corrosion resistance and microhardness of coatings [23], to give better mechanical properties than C 60 , when incorporated in poly(styrene-co-4-vinylpyridine), in catalysis [26][27][28], for optical limiting performance [24] or to reinforce and have antioxidation effects when mixed with natural rubber to inhibit the decrease of tensile strength after aging [25].…”
Section: Introductionmentioning
confidence: 99%
“…Because of their high solubility in water, these fullerene derivates represent attractive nanoparticles for various biological applications [1014]. In particular, fullerene and its derivates exhibit strong antioxidative, antimicrobial, cytoprotective, neuroprotective and radioprotective effects in animal organisms [10,1520]. …”
Section: Introductionmentioning
confidence: 99%
“…Fullerenols C 60 (OH) [18][19][20][21][22][23][24] have revealed maximal biological activity (4,7,8). Fullerenols demonstrated antioxidant activity, neutralizing reactive oxygen and nitrogen species (5,8,9), correcting neurological diseases (4,5,9,10), as well as functioning as radioprotectors (9) or antitumor agents (6).…”
Section: Introductionmentioning
confidence: 99%