TY - JOUR
T1 - Lead-Halide Perovskites for Photocatalytic α-Alkylation of Aldehydes
AU - Zhu, Xiaolin
AU - Lin, Yixiong
AU - Sun, Yue
AU - Beard, Matthew C.
AU - Yan, Yong
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/1/16
Y1 - 2019/1/16
N2 - Cost-effective and efficient photocatalysis are highly desirable in chemical synthesis. Here we demonstrate that readily prepared suspensions of APbBr 3 (A = Cs or methylammonium (MA)) type perovskite colloids (ca. 2-100 nm) can selectively photocatalyze carbon-carbon bond formation reactions, i.e., α-alkylations. Specifically, we demonstrate α-alkylation of aldehydes with a turnover number (TON) of over 52,000 under visible light illumination. Hybrid organic/inorganic perovskites are revolutionizing photovoltaic research and are now impacting other research fields, but their exploration in organic synthesis is rare. Our low-cost, easy-to-process, highly efficient and bandedge-tunable perovskite photocatalyst is expected to bring new insights in chemical synthesis.
AB - Cost-effective and efficient photocatalysis are highly desirable in chemical synthesis. Here we demonstrate that readily prepared suspensions of APbBr 3 (A = Cs or methylammonium (MA)) type perovskite colloids (ca. 2-100 nm) can selectively photocatalyze carbon-carbon bond formation reactions, i.e., α-alkylations. Specifically, we demonstrate α-alkylation of aldehydes with a turnover number (TON) of over 52,000 under visible light illumination. Hybrid organic/inorganic perovskites are revolutionizing photovoltaic research and are now impacting other research fields, but their exploration in organic synthesis is rare. Our low-cost, easy-to-process, highly efficient and bandedge-tunable perovskite photocatalyst is expected to bring new insights in chemical synthesis.
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U2 - 10.1021/jacs.8b08720
DO - 10.1021/jacs.8b08720
M3 - Article
AN - SCOPUS:85060110458
SN - 0002-7863
VL - 141
SP - 733
EP - 738
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 2
ER -