Lacunary Evolution of Molybdenum Blue Clusters for Efficient and Sustainable Photocatalytic Chemodivergent C─C Coupling Reactions

Y Yi Kuang (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China) Z Zhi‐Bin Mei (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China) J Jiao‐Min Lin (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China) C Cheng Zeng L Long‐Zhang Dong (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China) S Shao‐Hua Liang (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China) J Jing‐Wen Shi (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization, School of Chemistry South China Normal University Guangzhou P. R. China) L Lu Jin S Shun‐Li Li (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China) J Jiang Liu Y Ya‐Qian Lan (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China)

Abstract

ABSTRACT High‐nuclearity molybdenum blue (MB) clusters with regular lacunary variation are of great importance for polyoxometalate structure evolution and photocatalytic application study, but their synthesis still remains a huge challenge. Herein, we successfully synthesized a series of high‐nuclearity MB clusters, S 2 Mo 62 , SMo 53 W 7 , Mo 50 W 8 , and Mo 44 W 8 , which exhibit regular lacunary variation. More importantly, such structural variation endows these MB clusters with distinct Lewis acidity and redox properties. Consequently, when employed as heterogeneous photocatalysts for the chemodivergent C─C coupling reactions between 1,3‐diketones and alkenes, the hexa‐lacunary Mo 50 W 8 and Mo 44 W 8 with more Lewis acid sites can achieve a 93% 1,5‐diketone yield within 12 h, while parent S 2 Mo 62 with superior oxygen activation can achieve a 99% 1,4‐diketone yield within 3 h. Furthermore, Mo 50 W 8 enables gram‐scale and sunlight driven synthesis of diverse 1,5‐diketone, and maintains long‐term cycling stability over 370 h (16 cycles). This work represents the first report of high‐nuclearity MB clusters with regular lacunary variation, and extends their application to sunlight driven photocatalytic C─C coupling reaction, highlighting the innovative research of MB clusters.

Article Details

Volume / Issue Vol. 65, Issue 25
Published June 15, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

Y

Yi Kuang

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China

Z

Zhi‐Bin Mei

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China

J

Jiao‐Min Lin

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China

C

Cheng Zeng

L

Long‐Zhang Dong

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China

S

Shao‐Hua Liang

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China

J

Jing‐Wen Shi

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization, School of Chemistry South China Normal University Guangzhou P. R. China

L

Lu Jin

S

Shun‐Li Li

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China

J

Jiang Liu

Y

Ya‐Qian Lan

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China