The death of the Job plot, transparency, open science and online tools, uncertainty estimation methods and other developments in supramolecular chemistry data …

DB Hibbert, P Thordarson - Chemical Communications, 2016 - pubs.rsc.org
Data analysis is central to understanding phenomena in host–guest chemistry. We describe
here recent developments in this field starting with the revelation that the popular Job plot …

Electrochemically driven, Ni-catalyzed aryl amination: scope, mechanism, and applications

Y Kawamata, JC Vantourout, DP Hickey… - Journal of the …, 2019 - ACS Publications
C–N cross-coupling is one of the most valuable and widespread transformations in organic
synthesis. Largely dominated by Pd-and Cu-based catalytic systems, it has proven to be a …

A pentagonal cyanostar macrocycle with cyanostilbene CH donors binds anions and forms dialkylphosphate [3] rotaxanes

S Lee, CH Chen, AH Flood - Nature chemistry, 2013 - nature.com
Since the discovery of crown ethers, macrocycles have been recognized as powerful
platforms for supramolecular chemistry. Although their numbers and variations are now …

Anion binding in solution: beyond the electrostatic regime

Y Liu, A Sengupta, K Raghavachari, AH Flood - Chem, 2017 - cell.com
A fundamental understanding of anion binding by receptors is essential for managing salts
during energy, water, and food production. However, the limited understanding of solvent …

Halide Noninnocence and Direct Photoreduction of Ni (II) Enables Coupling of Aryl Chlorides in Dual Catalytic, Carbon–Heteroatom Bond-Forming Reactions

CH Chrisman, M Kudisch, KO Puffer… - Journal of the …, 2023 - ACS Publications
Recent mechanistic studies of dual photoredox/Ni-catalyzed, light-driven cross-coupling
reactions have found that the photocatalyst (PC) operates through either reductive …

Unified Photocatalytic Strategy for the Cross-Coupling of Alcohols with Aryl Halides Enabled by Synergistic Nickel and Iron LMCT Catalysis

M Jaber, Y Ozbay, E Chefdeville, G Tran… - ACS …, 2024 - ACS Publications
The use of alcohol feedstock as a coupling partner in cross-coupling reactions offers an
extraordinary potential for the efficient synthesis of Csp3-rich complex molecular scaffolds …

Flipping the switch on chloride concentrations with a light-active foldamer

Y Hua, AH Flood - Journal of the American Chemical Society, 2010 - ACS Publications
Here we demonstrate a bioinspired system where light stimulus is used to trigger the
wavelength-dependent release and then reuptake of chloride ions in nonaqueous solutions …

Hydrophobic collapse of foldamer capsules drives picomolar-level chloride binding in aqueous acetonitrile solutions

Y Hua, Y Liu, CH Chen, AH Flood - Journal of the American …, 2013 - ACS Publications
Aqueous media are competitive environments in which to perform host–guest chemistry,
particularly when the guest is highly charged. While hydrophobic binding is a recognized …

Revealing the hidden costs of organization in host–guest chemistry using chloride-binding foldamers and their solvent dependence

FC Parks, EG Sheetz, SR Stutsman… - Journal of the …, 2022 - ACS Publications
Preorganization is a key concept in supramolecular chemistry. Preorganized receptors
enhance binding by minimizing the organization costs associated with adopting the …

Mechanistic evidence of a Ni (0/II/III) cycle for nickel photoredox amide arylation

RD Bradley, BD McManus, JG Yam… - Angewandte Chemie …, 2023 - Wiley Online Library
This work demonstrates the dominance of a Ni (0/II/III) cycle for Ni‐photoredox amide
arylation, which contrasts with other Ni‐photoredox C‐heteroatom couplings that operate via …