More Like this

1. Reversible Cl ₂ /Cl ^– Redox for Low-Temperature Aqueous Batteries

   https://doi.org/10.1021/acsenergylett.2c02757  

   Sui, Yiming; Lei, Ming; Yu, Mingliang; Scida, Alexis; Sandstrom, Sean K.; Stickle, William; O’Larey, Timothy D.; Jiang, De-en; Ji, Xiulei (February 2023, ACS Energy Letters)
2. Mono- and disubstitution reactions of gyroscope like complexes derived from Cl Pt Cl rotators within cage like dibridgehead diphosphine ligands

   https://doi.org/10.1016/j.jorganchem.2016.03.022  

   Taher, Deeb; Nawara-Hultzsch, Agnieszka J.; Bhuvanesh, Nattamai; Hampel, Frank; Gladysz, John A. (October 2016, Journal of Organometallic Chemistry)
3. Generalized recursive atom ordering and equivalence to CL-shellability

   Hersh, Patricia; Stadnyk, Grace (July 2024, Combinatorial theory)
4. Reactivity of Chlorine Radicals (Cl ^• and Cl ₂ ^•– ) with Dissolved Organic Matter and the Formation of Chlorinated Byproducts

   https://doi.org/10.1021/acs.est.0c05596  

   Lei, Yu; Lei, Xin; Westerhoff, Paul; Zhang, Xinran; Yang, Xin (January 2021, Environmental Science & Technology)
5. Synthesis, characterization, and structure determination of Cp*Ir(dpms)Cl

   https://doi.org/10.1016/j.ica.2022.121210  

   Pohorenec, Ryan; Drelles, William G.; Cuneo, Daniel; Brennessel, William W.; Jones, William D. (September 2022, Inorganica Chimica Acta)

   Bipyridyl ligands are commonplace in catalysis. Structurally similar to this ligand class with unique properties is the novel di-(2-pyridyl)methanesulfonate (dpms) ligand, which is prepared and reacted with [Cp*IrCl2]2 to afford Cp*Ir(dpms)Cl (1) in high yield. Its single-crystal X-ray structure indicates an exo–(kappa2) conformation of the ligand, with the sulfonate group directed away from the iridium center. Halogen exchange by treatment of 1 with NaI gives the iodide derivative, Cp*Ir(dpms)I (2). Abstraction of the halogen from 1 using AgPF6 generates [Cp*Ir(dpms)]PF6 (3), which was not found to activate the C-H bonds of benzene. 

   more » « less