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Carson J. Bruns

Researcher at University of Colorado Boulder

Publications -  59
Citations -  3232

Carson J. Bruns is an academic researcher from University of Colorado Boulder. The author has contributed to research in topics: Rotaxane & Supramolecular chemistry. The author has an hindex of 23, co-authored 48 publications receiving 2752 citations. Previous affiliations of Carson J. Bruns include Northwestern University & University of Liège.

Papers
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A Naphthodithiophene-Diketopyrrolopyrrole Donor Molecule for Efficient Solution-Processed Solar Cells

TL;DR: The synthesis, characterization, and first implementation of a naphtho[2,3-b:6,7-b']dithiophene (NDT)-based donor molecule in highly efficient organic photovoltaics (OPVs) is reported.
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Rotaxane-Based Molecular Muscles

TL;DR: It is emphasized how rotaxanes constitute a remarkably versatile platform for directing force and motion, owing to the wide range of stimuli that can be used to actuate them and their diverse modes of mechanical switching as dictated by the stereochemistry of their mechanical bonds.
Book

The Nature of the Mechanical Bond: From Molecules to Machines

TL;DR: The Nature of the Mechanical Bond as mentioned in this paper is a comprehensive review of much of the contemporary literature on the mechanical bond, accessible to newcomers and veterans alike, including Supramolecular, covalent, and statistical approaches to the formation of entanglements that underpin mechanical bonds in molecules and macromolecules.
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Tunable solid-state fluorescent materials for supramolecular encryption

TL;DR: This work describes a heterorotaxane with tunable solid-state fluorescent emissions enabled through reversible manipulation of its aggregation by supramolecular encapsulation, which constitutes a unique application of responsive complex equilibria in the form of a cryptographic algorithm that protects valuable information printed using tunable Solid State fluorescent materials.
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ExBox: A Polycyclic Aromatic Hydrocarbon Scavenger

TL;DR: A template-directed protocol is employed to synthesize a semi-rigid cyclophane that adopts a box-like geometry and is comprised of π-electron-poor 1,4-phenylene-bridged ("extended") bipyridinium units (ExBIPY(2+)), resulting in the isolation of different aromatic compounds after ExBox·4Cl was regenerated.