In this review, a summary of transition metal-catalyzed C–H activation by utilizing the functionalities as directing groups is presented.

：CdS is a very good visible-light responsive photocatalyst for hydrogen production. However, the fast recombination of photogenerated electron-hole pairs and quick photocorrosion limit its application in photocatalysis. To address these problems, we herein have designed and synthesized monodisperse polyaniline@cadmium sulfide (PANI@CdS) core-shell nanospheres to probe the mechanisms of photocorrosion inhibition and photocatalytic H 2 production. All the PANI@CdS core-shell nanospheres demonstrate highly enhanced photocorrosion inhibition and photocatalytic hydrogen production comparing to the pure CdS nanospheres. Particularly, the PANI@CdS core-shell nanospheres with the thinnest PANI shell possess the highest hydrogen production rate of 310 μmol h-1 g-1 in 30 h without deactivation. Our results reveal that the newly formed C-S and/or N-Cd bonds in PANI@CdS prevent the reduction of the surface sulfide ions to sulphur, leading to effective photocorrosion inhibition. Our results also verify that the photogenerated holes migrating from valence band (VB) of CdS to the highest occupied molecular orbital (HOMO) of PANI leads to the enhanced photocatalytic hydrogen production. This work can shed some light on the mechanism of conducting polymers modifying metal sulfides for effective photocorrosion inhibition and highly enhanced photocatalytic activities.

MnO2 nanosheet functionalized S@PEDOT core–shell nanospheres demonstrate highly enhanced electrochemical performance for Li–S batteries, benefitting from effectively trapping polysulfides, minimizing polysulfide dissolution, and improving cathode conductivity and wettability.