The n→π* Interaction

RW Newberry, RT Raines - Accounts of chemical research, 2017 - ACS Publications
Conspectus The carbonyl group holds a prominent position in chemistry and biology not
only because it allows diverse transformations but also because it supports key …

The n→ π* interaction: a rapidly emerging non-covalent interaction

SK Singh, A Das - Physical Chemistry Chemical Physics, 2015 - pubs.rsc.org
This perspective describes the current status of a recently discovered non-covalent
interaction named as the n→ π* interaction, which is very weak and counterintuitive in …

Applications of discrete synthetic macromolecules in life and materials science: recent and future trends

R Aksakal, C Mertens, M Soete, N Badi… - Advanced …, 2021 - Wiley Online Library
In the last decade, the field of sequence‐defined polymers and related ultraprecise,
monodisperse synthetic macromolecules has grown exponentially. In the early stage, mainly …

Sequence programmable peptoid polymers for diverse materials applications

AS Knight, EY Zhou, MB Francis… - Advanced …, 2015 - Wiley Online Library
Polymer sequence programmability is required for the diverse structures and complex
properties that are achieved by native biological polymers, but efforts towards controlling the …

Intrinsically fluorescent polyureas toward conformation-assisted metamorphosis, discoloration and intracellular drug delivery

Y Zhou, F Fan, J Zhao, Z Wang, R Wang… - Nature …, 2022 - nature.com
Peptidomimetic polymers have attracted increasing interest because of the advantages of
facile synthesis, high molecular tunability, resistance to degradation, and low …

Oligo (maleic anhydride) s: a platform for unveiling the mechanism of clusteroluminescence of non-aromatic polymers

X Zhou, W Luo, H Nie, L Xu, R Hu, Z Zhao… - Journal of Materials …, 2017 - pubs.rsc.org
Luminescent materials without conventional aromatic groups have attracted extensive
attention in recent years. However, the luminescence mechanism has been obscure and …

Structure–function relationships in peptoids: recent advances toward deciphering the structural requirements for biological function

SA Fowler, HE Blackwell - Organic & biomolecular chemistry, 2009 - pubs.rsc.org
Oligomers of N-substituted glycine, or peptoids, are versatile tools to probe biological
processes and hold promise as therapeutic agents. An underlying theme in the majority of …

n→π* Interactions of Amides and Thioamides: Implications for Protein Stability

RW Newberry, B VanVeller, IA Guzei… - Journal of the American …, 2013 - ACS Publications
Carbonyl–carbonyl interactions between adjacent backbone amides have been implicated
in the conformational stability of proteins. By combining experimental and computational …

Nature of amide carbonyl− carbonyl interactions in proteins

A Choudhary, D Gandla, GR Krow… - Journal of the American …, 2009 - ACS Publications
Noncovalent interactions define and modulate biomolecular structure, function, and
dynamics. In many protein secondary structures, an intimate interaction exists between …

Extraordinarily Robust Polyproline Type I Peptoid Helices Generated via the Incorporation of α-Chiral Aromatic N-1-Naphthylethyl Side Chains

JR Stringer, JA Crapster, IA Guzei… - Journal of the American …, 2011 - ACS Publications
Peptoids, or oligomers of N-substituted glycines, are a class of foldamers that have shown
extraordinary functional potential since their inception nearly two decades ago. However …