Photochemical syntheses of fullerene-amine adducts and their characterization with 1H NMR spectroscopy

Motomichi Inoue; Lorena Machi; Francisco Brown; Michiko B. Inoue; Quintus Fernando

doi:10.1016/0022-2860(94)08395-X

Photochemical syntheses of fullerene-amine adducts and their characterization with ¹H NMR spectroscopy

Motomichi Inoue^*
, Lorena Machi
, Francisco Brown
, Michiko B. Inoue
, Quintus Fernando

^*Corresponding author for this work

Departamento de Investigación en Polímeros y Materiales

Research output: Contribution to journal › Article › peer-review

10 Scopus citations

Abstract

Photoreactions of C₆₀ with aromatic or aliphatic amines in contact with air gave a new type of amine adduct with a general compound formula of C₆₀(amine)_x(OH)_yO_z; the amine was di-2-pyridylamine, morpholine or N,N-dimethylethylenediamine. The N,N-dimethylethylenediamine adduct was obtained as a hydrochloride. Its ¹H NMR spectrum showed that the adduct cation, obtained after functionalizing C₆₀, formed an ion pair with a benzenesulfonate anion.

Original language	English
Pages (from-to)	113-117
Number of pages	5
Journal	Journal of Molecular Structure
Volume	345
DOIs	https://doi.org/10.1016/0022-2860(94)08395-X
State	Published - 1995

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title = "Photochemical syntheses of fullerene-amine adducts and their characterization with 1H NMR spectroscopy",

abstract = "Photoreactions of C60 with aromatic or aliphatic amines in contact with air gave a new type of amine adduct with a general compound formula of C60(amine)x(OH)yOz; the amine was di-2-pyridylamine, morpholine or N,N-dimethylethylenediamine. The N,N-dimethylethylenediamine adduct was obtained as a hydrochloride. Its 1H NMR spectrum showed that the adduct cation, obtained after functionalizing C60, formed an ion pair with a benzenesulfonate anion.",

author = "Motomichi Inoue and Lorena Machi and Francisco Brown and Inoue, \{Michiko B.\} and Quintus Fernando",

year = "1995",

doi = "10.1016/0022-2860(94)08395-X",

language = "Ingl{\'e}s",

volume = "345",

pages = "113--117",

journal = "Journal of Molecular Structure",

issn = "0022-2860",

publisher = "Elsevier BV",

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TY - JOUR

T1 - Photochemical syntheses of fullerene-amine adducts and their characterization with 1H NMR spectroscopy

AU - Inoue, Motomichi

AU - Machi, Lorena

AU - Brown, Francisco

AU - Inoue, Michiko B.

AU - Fernando, Quintus

PY - 1995

Y1 - 1995

N2 - Photoreactions of C60 with aromatic or aliphatic amines in contact with air gave a new type of amine adduct with a general compound formula of C60(amine)x(OH)yOz; the amine was di-2-pyridylamine, morpholine or N,N-dimethylethylenediamine. The N,N-dimethylethylenediamine adduct was obtained as a hydrochloride. Its 1H NMR spectrum showed that the adduct cation, obtained after functionalizing C60, formed an ion pair with a benzenesulfonate anion.

AB - Photoreactions of C60 with aromatic or aliphatic amines in contact with air gave a new type of amine adduct with a general compound formula of C60(amine)x(OH)yOz; the amine was di-2-pyridylamine, morpholine or N,N-dimethylethylenediamine. The N,N-dimethylethylenediamine adduct was obtained as a hydrochloride. Its 1H NMR spectrum showed that the adduct cation, obtained after functionalizing C60, formed an ion pair with a benzenesulfonate anion.

UR - https://www.scopus.com/pages/publications/0042513118

U2 - 10.1016/0022-2860(94)08395-X

DO - 10.1016/0022-2860(94)08395-X

M3 - Artículo

SN - 0022-2860

VL - 345

SP - 113

EP - 117

JO - Journal of Molecular Structure

JF - Journal of Molecular Structure

ER -

Photochemical syntheses of fullerene-amine adducts and their characterization with ¹H NMR spectroscopy

Abstract

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