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Journal ArticleDOI

Single-Event Spectroscopy and Unravelling Kinetics of Covalent Domains Based on Cyclobutane Mechanophores

TLDR
In this paper, a covalent synthetic mimics of the mechanical unfolding of noncovalent “stored length” doma... is proposed to serve as a synthetic mimic of the unfolding of polymer contour length.
Abstract
Mechanochemical reactions that lead to an increase in polymer contour length have the potential to serve as covalent synthetic mimics of the mechanical unfolding of noncovalent “stored length” doma...

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Citations
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Journal ArticleDOI

Force-Induced Near-Infrared Chromism of Mechanophore-Linked Polymers.

TL;DR: In this article, a mechanophore based on benzo[1,3]oxazine (OX) fused with a heptamethine cyanine moiety was developed and incorporated into a poly(methyl acrylate) chain to showcase the first force-induced NIR chromism in polymeric materials.
Journal ArticleDOI

Understanding the Mechanochemistry of Ladder-Type Cyclobutane Mechanophores by Single Molecule Force Spectroscopy.

TL;DR: In this paper, a series of ladder-type cyclobutane mechanophores, polymers of which can transform from nonconjugated structures to conjugated structures and change many properties at once, are reported.
Journal ArticleDOI

Exploration of Metal-Ligand Coordination Bonds in Proteins by Single-molecule Force Spectroscopy

TL;DR: It is shown that metalloprotein plays an essential role in many different biological processes and represents an indispensable protein subgroup and the knowledge of this subgroup is essential for the development of new drugs to treat cancer.
Journal ArticleDOI

Force Dependent Barriers from Analytic Potentials within Elastic Environments

TL;DR: In this article , it is shown that solely elastic environments do not change this barrier in contrast to the predictions of constraint geometry simulate external force (COGEF) strategies, which is confirmed by explicit calculations of bond rupture in a polydimethylsiloxane model.
Journal ArticleDOI

Covalent Mechanochemistry and Contemporary Polymer Network Chemistry: A Marriage in the Making.

TL;DR: In this paper , the potential match between covalent polymer mechanochemistry and recent advances in polymer network chemistry, specifically, topologically controlled networks and the hierarchical material responses enabled by multi-network architectures and mechanically interlocked polymers is discussed.
References
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Journal ArticleDOI

Three concomitant C–C dissociation pathways during the mechanical activation of an N-heterocyclic carbene precursor

TL;DR: The mechanical dissociation of an N-heterocyclic carbene precursor has been shown to proceed with the rupture of a C–C bond through concomitant heterolytic, concerted and homolytic pathways.
Journal ArticleDOI

Accelerating a Mechanically Driven anti-Woodward–Hoffmann Ring Opening with a Polymer Lever Arm Effect

TL;DR: It is shown that a polymer "lever arm effect" can provide a mechanical advantage in accelerating the symmetry forbidden disrotatory ring opening of benzocyclobutene (BCB).
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A Polymer with Mechanochemically Active Hidden Length.

TL;DR: The advantages of adding mechanochemical reactivity to hidden length itself are demonstrated, using a new mechanophore that integrates (Z)-2,3-diphenylcyclobutene-1,4-dicarboxylate, with hitherto unknown mechanochemistry, into macrocyclic cinnamate dimers.
Journal ArticleDOI

Comparison of the predictive performance of the Bell-Evans, Taylor-expansion and statistical-mechanics models of mechanochemistry.

TL;DR: Comparison with results obtained from quantum-chemical calculations of complete conformational ensembles coupled to a stretching force reveal that the simplest model yields qualitatively accurate results at minimal computational expense.
Journal ArticleDOI

Bicyclohexene-peri-naphthalenes: Scalable Synthesis, Diverse Functionalization, Efficient Polymerization, and Facile Mechanoactivation of Their Polymers.

TL;DR: Poly(BCH-Naph)s represent an attractive polymechanophore system to explore multifaceted mechanical response in solution and solid states, owing to the synthetic scalability, functional diversity, efficient polymerization, and facile mechanoactivation.
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