ABSTRACT
Understanding the ice recrystallization inhibition (IRI) mechanism is of fundamental importance for the rational design of novel antifreeze protein mimetics and reducing IR-related damage. In this communication, using quantitive experimental methods and molecular dynamics simulations we demonstrate that zwitterionic poly(carboxybetaine methacrylate) (PCBMA) can serve as a novel IRI-active substance. This work unravels the atomic-level details of the IRI mechanism of zwitterionic antifreeze protein mimetics and provides insight into the development of next-generation antifreeze protein mimetics.
ABSTRACT
Desilylative coupling involving C-Si bond cleavage has emerged as one of the most important synthetic strategies for carbon-carbon/heteroatom bond formation in solution chemistry. However, in on-surface chemistry, C-Si bond cleavage remains a synthetic challenge. Here, we report the implementation of C(sp2)-Si bond cleavage and subsequent C-C bond formation on metal surfaces. The combination of scanning tunneling microscopy and density functional theory calculation successfully reveals that the incorporation of the C-Br group on the arylsilanes is critical to the success of this desilylative coupling reaction on metal surfaces. Our study represents a promising approach for the removal of protecting silyl groups in on-surface chemistry.
Subject(s)
Carbon , Microscopy, Scanning Tunneling , Carbon/chemistry , MetalsABSTRACT
The high cost of noble metal catalysts has been a major factor limiting their industrial applications. It is thus of strong interest to develop catalysts with minimum metal loading. Here, we designed and prepared a single-atom ruthenium catalyst through a cascade anchoring strategy to maximize the efficiency of Ru atoms for acetylene hydrochlorination. The single-atom catalyst supported on commercial activated carbon (AC) exhibits excellent catalytic activity with acetylene conversion of 95.4% at an acetylene gas hourly space velocity (GHSV) of 720 h-1 and almost no deactivation during a 600 h catalyst lifetime test. In conjunction with a series of experimental characterizations of the catalyst, including aberration-corrected scanning transmission electron microscopy (Ac-STEM), X-ray photoelectron spectroscopy (XPS), and extended X-ray absorption fine spectroscopy (EXAFS), density functional theory (DFT) study shows that RuN4 sites are likely responsible for acetylene hydrochlorination catalytic activity. This work provides a strategy to design efficient single-atom catalysts for acetylene hydrochlorination and helps us to gain deeper understanding of single-atom catalytic mechanisms.