Home / Publications / Synthesis and characterization of a potential bifunctional C60-Ih fullerene-based catechol amide ligand

Synthesis and characterization of a potential bifunctional C60-Ih fullerene-based catechol amide ligand

Qingchun Zhang 1
Qingchun Zhang
, 
Bo Jin 1
Bo Jin
, 
Rufang Peng 1
Rufang Peng
, 
Shan Lei 1
Shan Lei
, 
Shijin Chu 1
Shijin Chu
10.1016/j.mencom.2015.05.015
Published 2015-04-28
Communication , Volume 25, Issue 3, 204-206
7
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Zhang Q. et al. Synthesis and characterization of a potential bifunctional C60-Ih fullerene-based catechol amide ligand // Mendeleev Communications. 2015. Vol. 25. No. 3. pp. 204-206.
GOST all authors (up to 50) Copy
Zhang Q., Jin B., Peng R., Lei S., Chu S. Synthesis and characterization of a potential bifunctional C60-Ih fullerene-based catechol amide ligand // Mendeleev Communications. 2015. Vol. 25. No. 3. pp. 204-206.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2015.05.015
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.05.015
TI - Synthesis and characterization of a potential bifunctional C60-Ih fullerene-based catechol amide ligand
T2 - Mendeleev Communications
AU - Zhang, Qingchun
AU - Jin, Bo
AU - Peng, Rufang
AU - Lei, Shan
AU - Chu, Shijin
PY - 2015
DA - 2015/04/28
PB - Mendeleev Communications
SP - 204-206
IS - 3
VL - 25
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2015_Zhang,
author = {Qingchun Zhang and Bo Jin and Rufang Peng and Shan Lei and Shijin Chu},
title = {Synthesis and characterization of a potential bifunctional C60-Ih fullerene-based catechol amide ligand},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.05.015},
number = {3},
pages = {204--206},
doi = {10.1016/j.mencom.2015.05.015}
}
MLA
Cite this
MLA Copy
Zhang, Qingchun, et al. “Synthesis and characterization of a potential bifunctional C60-Ih fullerene-based catechol amide ligand.” Mendeleev Communications, vol. 25, no. 3, Apr. 2015, pp. 204-206. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.05.015.

Abstract

The new C60-Ih fullerene-based catechol amide derivatives C60{C[COO(CH2)nCAM]2} [n = 2, 3 or 4; CAM = 2,3-Ph(OH)2CONH] were prepared using a modified Bingel-type reaction of C60-Ih and characterized by variable-temperature 1H NMR spectroscopy.

References

1.
P. Galle, Toxiques Nucléaires, Masson, Paris, 1997, pp. 185-209.
3.
10.1016/j.mencom.2015.05.015_bib0015
Durbin
2006
4.
10.1016/j.mencom.2015.05.015_bib0020
Pellmar
Neurotoxicology, 1999
5.
Uranium induces oxidative stress in lung epithelial cells
Periyakaruppan A., Kumar F., Sarkar S., Sharma C.S., Ramesh G.T.
Archives of Toxicology, 2006
7.
Rational Design of Sequestering Agents for Plutonium and Other Actinides
Gorden A.E., Xu J., Raymond K.N., Durbin P.
Chemical Reviews, 2003
8.
Sequestering agent for uranyl chelation: a new family of CAMS ligands
Leydier A., Lecerclé D., Pellet-Rostaing S., Favre-Reguillon A., Taran F., Lemaire M.
Tetrahedron, 2008
9.
Sequestering agents for uranyl chelation: new calixarene ligands
Leydier A., Lecerclé D., Pellet-Rostaing S., Favre-Réguillon A., Taran F., Lemaire M.
Tetrahedron, 2008
10.
C. D. Gutsche, in Calixarenes Revisited. Monographs in Supramolecular Chemistry, ed. J. F. Stoddart, The Royal Society of Chemistry, Cambridge, 1998, vol. 6.
11.
Sequestering agent for uranyl chelation: new binaphtyl ligands
Leydier A., Lecerclé D., Pellet-Rostaing S., Favre-Reguillon A., Taran F., Lemaire M.
Tetrahedron Letters, 2011
12.
EDTA and DTPA modified ligands as sequestering agents for uranyl decorporation
Leydier A., Lin Y., Arrachart G., Turgis R., Lecerclé D., Favre-Reguillon A., Taran F., Lemaire M., Pellet-Rostaing S.
Tetrahedron, 2012
13.
10.1016/j.mencom.2015.05.015_bib0065
Andrievsky
Med., 2009
14.
Radical Reactions of C60
Krusic P.J., Wasserman E., Keizer P.N., Morton J.R., Preston K.F.
Science, 1991
15.
Fullerene-based antioxidants and neurodegenerative disorders.
Dugan L.L., Lovett E.G., Quick K.L., Lotharius J., Lin T.T., O'Malley K.L.
Parkinsonism and Related Disorders, 2001
17.
The scavenging of reactive oxygen species and the potential for cell protection by functionalized fullerene materials
Yin J., Lao F., Fu P.P., Wamer W.G., Zhao Y., Wang P.C., Qiu Y., Sun B., Xing G., Dong J., Liang X., Chen C.
Biomaterials, 2009
19.
Kornev A.B., Peregudov A.S., Martynenko V.M., Guseva G.V., Sashenkova T.E., Rybkin A.Y., Faingold I.I., Mishchenko D.V., Kotelnikova R.A., Konovalova N.P., Balzarini J., Troshin P.A.
Mendeleev Communications, 2013
22.
Efficient cyclopropanation of C60 starting from malonates
Camps X., Hirsch A.
Journal of the Chemical Society Perkin Transactions 1, 1997
23.
Preparation and Characterization of Fulleroid and Methanofullerene Derivatives
Hummelen J.C., Knight B.W., LePeq F., Wudl F., Yao J., Wilkins C.L.
Journal of Organic Chemistry, 1995
24.
Structure of C60 fullerene in water: spectroscopic data
Scharff P., Risch K., Carta-Abelmann L., Dmytruk I.M., Bilyi M.M., Golub O.A., Khavryuchenko A.V., Buzaneva E.V., Aksenov V.L., Avdeev M.V., Prylutskyy Y.I., Durov S.S.
Carbon, 2004
26.
Syntheses, structures, and properties of methanofullerenes
Diederich F., Isaacs L., Philp D.
Chemical Society Reviews, 1994
27.
Internal Motions in a Fulleropyrrolidine Tertiary Amide with Axial Chirality
Borsato G., Negra F.D., Gasparrini F., Misiti D., Lucchini V., Possamai G., Villani C., Zambon A.
Journal of Organic Chemistry, 2004
28.
[60]Fullerene as a Substituent
Bagno A., Claeson S., Maggini M., Martini M.L., Prato M., Scorrano G.
Chemistry - A European Journal, 2002
29.
Highly-iodinated fullerene as a contrast agent for X-ray imaging.
Wharton T., Wilson L.J.
Bioorganic and Medicinal Chemistry, 2002