Modulation of the exfoliated graphene work function through cycloaddition of nitrile imines

被引:16
|
作者
Barrejon, Myriam [1 ]
Gomez-Escalonilla, Maria J. [1 ]
Fierro, Jose Luis G. [2 ]
Prieto, Pilar [3 ]
Carrillo, Jose R. [3 ]
Rodriguez, Antonio M. [3 ,4 ]
Abellan, Gonzalo [5 ,6 ,7 ]
Cruz Lopez-Escalante, Ma [8 ]
Gabas, Mercedes [9 ]
Lopez-Navarrete, Juan T. [10 ]
Langa, Fernando [1 ]
机构
[1] Univ Castilla La Mancha, Inst Nanociencia Nanotecnol & Mat Mol INAMOL, Toledo 45071, Spain
[2] CSIC, Inst Catalisis & Petroleoquim, Plaza Murillo 2, E-28049 Madrid, Spain
[3] Univ Castilla La Mancha, Fac Ciencias & Tecnol Quim, Dept Quim Organ Inorgan & Bioquim, Campus Univ, E-13071 Ciudad Real, Spain
[4] Univ Napoli Federico II, Dipartimento Sci Chim, Via Cintia, I-80126 Naples, Italy
[5] Friedrich Alexander Univ Erlangen Nurnberg, Dept Chem & Pharm, Henkestr 42, D-91054 Erlangen, Germany
[6] Friedrich Alexander Univ Erlangen Nurnberg, Inst Adv Mat & Proc ZMP, Henkestr 42, D-91054 Erlangen, Germany
[7] Dr Mack Str 81, D-90762 Furth, Germany
[8] Univ Malaga, Lab Mat & Superficies, Dept Ingn Quim, Unidad Nanotecnol, E-29071 Malaga, Spain
[9] Univ Malaga, Lab Mat & Superficies, Dept Fis Aplicada 1, Unidad Nanotecnol, E-29071 Malaga, Spain
[10] Univ Malaga, Dept Phys Chem, Campus Teatinos S-N, E-29071 Malaga, Spain
关键词
MOLECULAR-ORBITAL METHODS; WALL CARBON NANOTUBES; GAUSSIAN-TYPE BASIS; ELECTRON-TRANSFER; COVALENT FUNCTIONALIZATION; DENSITY FUNCTIONALS; AZOMETHINE YLIDES; CHEMISTRY; OXIDE; STABILITY;
D O I
10.1039/c6cp05285a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
After the feasibility of the 1,3-dipolar cycloaddition reaction between nitrile imines and exfoliated graphene by density functional theory calculations was proved, very few-layer graphene was effectively functionalized using this procedure. Hydrazones with different electronic properties were used as precursors for the 1,3-dipoles, and microwave irradiation as an energy source enabled the reaction to be performed in a few minutes. The anchoring of organic addends on the graphene surface was confirmed by Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis. Ultraviolet photoelectron spectroscopy (UPS) was used to measure the work function and band gap of these new hybrids. Our results demonstrate that it is possible to modulate these important electronic valence band parameters by tailoring the electron richness of the organic addends and/or the degree of functionalization.
引用
收藏
页码:29582 / 29590
页数:9
相关论文
共 50 条
  • [1] CYCLOADDITION OF NITRILE IMINES TO CYCLOOCTATETRAENE
    BIANCHI, G
    GANDOLFI, R
    GRUNANGE.P
    TETRAHEDRON, 1973, 29 (16) : 2405 - 2410
  • [2] SYNTHESIS OF FUSED RING 1,2,4-TRIAZOLES BY INTRAMOLECULAR CYCLOADDITION OF NITRILE IMINES TO NITRILE FUNCTION
    GARANTI, L
    SCANDROGLIO, A
    ZECCHI, G
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1976, 13 (06) : 1339 - 1341
  • [3] Sulfonyl pyrazoles and isoxazoles: Cycloaddition of nitrile imines and nitrile oxides to aryl styryl sulfones
    Padmavathi, V
    Reddy, AVB
    Sumathi, RP
    Padmaja, A
    Reddy, DB
    INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 1998, 37 (12): : 1286 - 1289
  • [4] 1,3-Dipolar cycloaddition of nitrile imines to meso-tetraarylporphyrins
    Moura, Nuno M. M.
    Giuntini, F.
    Faustino, Maria A. F.
    Neves, Maria G. P. M. S.
    Tome, Augusto C.
    Silva, Artur M. S.
    Rakib, E. M.
    Hannioui, A.
    Abouricha, S.
    Roeder, Beate
    Cavaleiro, Jose A. S.
    ARKIVOC, 2010, : 24 - 33
  • [5] 1,3-Dipolar Cycloaddition Reaction of Nitrile Oxides to Isatin Imines
    Souzangarzadeh, Saeid
    IRANIAN JOURNAL OF CHEMISTRY & CHEMICAL ENGINEERING-INTERNATIONAL ENGLISH EDITION, 2016, 35 (01): : 31 - 35
  • [6] Functionalization of Graphene with Nitrile Groups by Cycloaddition of Tetracyanoethylene Oxide
    Peng, Xiaojun
    Li, Yang
    Zhang, Guoliang
    Zhang, Fengbao
    Fan, Xiaobin
    JOURNAL OF NANOMATERIALS, 2013, 2013
  • [7] Cycloaddition of Nitrile Oxides to Graphene: a Theoretical and Experimental Approach
    Uceta, Helena
    Vizuete, Maria
    Carrillo, Jose R.
    Barrejon, Myriam
    Fierro, Jose Luis G.
    Pilar Prieto, Maria
    Langa, Fernando
    CHEMISTRY-A EUROPEAN JOURNAL, 2019, 25 (64) : 14644 - 14650
  • [8] INTRAMOLECULAR CARBENE-TYPE 1,1-CYCLOADDITION BY NITRILE IMINES
    GARANTI, L
    VIGEVANI, A
    ZECCHI, G
    TETRAHEDRON LETTERS, 1976, (18) : 1527 - 1528
  • [9] Cycloaddition of nitrile imines and Diels-Alder reaction of anthracene to isoxazolyl maleimides
    Rajanarendar, E
    Srinivas, M
    Karunakar, D
    Ramu, K
    HETEROCYCLIC COMMUNICATIONS, 2005, 11 (05) : 441 - 444
  • [10] An entry to a chiral dihydropyrazole scaffold: Enantioselective [3 + 2] cycloaddition of nitrile imines
    1600, American Chemical Society, Columbus, United States (127):