Southern University of Science and Technology, China
Xumu Zhang received his BS from Wuhan University (1982) and MS from Chinese Science Academy (1985) with Professor Jiaxi Lu and University of California, San Diego (1987) with Professor Gerhard N. Schrauzer. He received his Ph.D. in chemistry in 1992 from Stanford University under the guidance of Professor James P. Collman (The supervisor of Nobel Prize winner K. Barry Sharpless and Robert H. Grubbs). He pursued postdoctoral research at Stanford University from 1992 to 1994. Before joining SUSTech as the first chairman of chemistry department in 2015, he was a professor of chemistry in Pennstate University and distinguished professor in Rutgers University.
In 2002, Xumu Zhang became the first person from mainland China to be honored with the prestigious ACS Cope Scholar Award. He was recognized for his groundbreaking invention of the chiral ligands' toolbox, which facilitated the development of homogeneous catalysts, enabling the practical synthesis of numerous chiral molecules, particularly those of great biological significance. In 2014, an efficient ring-forming chemical reaction known as the "Zhang Enyne Cycloisomerization" was named after him, and has been documented in the book Strategic Applications of Named Reactions in Organic Synthesis. In 2016, he was awarded as Asian Core Program (ACP) Lectureship. In 2022, he was elected as a foreign member of the Russian Academy of Sciences, and received Evonik Chemical Innovation Award Outstanding Scientist (one per year).
In frontier areas of science, Xumu Zhang has applied over 50 U.S. and international patents, published more than 400 papers and the papers are cited over 25000 times. One of his notable achievements includes the development of privileged, powerful, and practical chiral ligands for asymmetric catalysis. These ligands have enabled promising industrial applications, particularly in the synthesis of drug molecules. Recently, he developed a new type of ligands designed for use as metalorganocatalyst. These ligands possess dual activating modes, combining the strengths of metal catalysis and organocatalysis. This innovative approach opens up new possibilities in catalytic reactions.