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1.
J Nanosci Nanotechnol ; 21(10): 5370-5377, 2021 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-33875131

RESUMO

Hierarchical TiO2-Bi2MoO6 nanospheres as efficient visible-light responsive photocatalyst are fabricated by dispersing brookite TiO2 nanorods on the hierarchical Bi2MoO6 nanospheres, which provides visible-light absorption and large surface area. The morphologies, surface area and light absorption features of as-prepared TiO²-Bi²MoO6 can be rational controlled by varying the loading amount of TiO² nanorods on hierarchical Bi²MoO6 nanospheres. As a result, the TiO²-Bi²MoO6-3 yields 380 ppm CO² production for decomposing 2-propanol at 11 h under visible light irradiation, realizing 4.4 times enhancement of photocatalytic property with respect to pure TiO² nanorods. Moreover, the three-dimensional hierarchical architecture enables the hybrid TiO²-Bi²MoO6 excellent cycling stability.

2.
Org Biomol Chem ; 16(28): 5197-5202, 2018 07 18.
Artigo em Inglês | MEDLINE | ID: mdl-29972191

RESUMO

An efficient iodocarbocyclization of alkenes for the synthesis of iodooxindoles has been developed. This reaction proceeds in a chemoselective manner and shows excellent tolerance of various functional groups, including a chemosensitive hydroxymethyl group. Nonmetal inorganic iodine pentoxide was used as both the oxidant and iodine source, making this protocol very practical. On the basis of experimental observations, a plausible electrophilic reaction mechanism was proposed.

3.
J Org Chem ; 83(4): 2369-2375, 2018 02 16.
Artigo em Inglês | MEDLINE | ID: mdl-29400062

RESUMO

An efficient oxidative aminooxyarylation of alkenes under a transition-metal-free condition was described. Under the reaction conditions, N-hydroxyphthalimide (NHPI) reacted readily with N-arylacrylamides to produce cyclic products via a radical C-H functionalization process, achieving both C-O and C-C bonds formation in one pot. This reaction provided a facile access to the valuable aminooxylated oxindoles. The benzylic and α-methylene C(sp3)-H bonds were also aminooxylated under the reaction conditions.


Assuntos
Alcenos/química , Indóis/síntese química , Indóis/química , Estrutura Molecular , Oxirredução , Oxindóis
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