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Journal ArticleDOI

exTTF as a Building Block for Fullerene Receptors. Unexpected Solvent-Dependent Positive Homotropic Cooperativity

TLDR
The first exTTF-based receptor for molecular recognition of fullerene is described, which shows completely different binding modes in chlorobenzene and CHCl3/CS2 mixtures.
Abstract
The first exTTF-based receptor for molecular recognition of fullerene is described. Unexpectedly, the receptor shows completely different binding modes in chlorobenzene and CHCl3/CS2 mixtures. In the aromatic solvent, the receptor binds C60 in a noncooperative fashion (nH = 1) with a Kassoc = (2.98 ± 0.12) × 103 M-1, whereas in CHCl3/CS2 mixtures, it shows a marked positive homotropic cooperative effect (nH = 2.7) toward binding of C60, with an apparent binding constant of (3.56 ± 0.16) × 103 M-1. The unique solvent-switchable behavior of our receptor might find use in the controlled self-assembly of exTTF−C60 donor−acceptor ensembles.

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Artificial Molecular Machines

TL;DR: The latest generations of sophisticated synthetic molecular machine systems in which the controlled motion of subcomponents is used to perform complex tasks are discussed, paving the way to applications and the realization of a new era of “molecular nanotechnology”.
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Tetrathiafulvalene (TTF) derivatives: key building-blocks for switchable processes

TL;DR: Recent developments of TTF-based molecular and supramolecular systems in this respect are discussed, including molecular sensors, redox-fluorescent switches, multi-input systems for logic gates, electrochemically-driven conformational controls, molecular clips and tweezers, andRedox-controlled gelation processes.
Journal ArticleDOI

Selective prepared carbon nanomaterials for advanced photocatalytic application in environmental pollutant treatment and hydrogen production

TL;DR: In this article, a review of carbon nanomaterials (CNMs)-modified photocatalysts is presented, which provides a wide view of recent preparation methods, applications, prospects and challenges.
Journal ArticleDOI

Electronic Communication in Tetrathiafulvalene (TTF)/C60 Systems: Toward Molecular Solar Energy Conversion Materials?

TL;DR: The covalent connection of the electron acceptor C 60 to p-quinonoid pi-extended tetrathiafulvalenes (exTTFs) has allowed for the preparation of new photo- and electroactive conjugates able to act as artificial photosynthetic systems and active molecular materials in organic photovoltaics.
Journal ArticleDOI

Curves ahead: molecular receptors for fullerenes based on concave-convex complementarity.

TL;DR: This tutorial review presents a brief overview of the recent advances in the construction of molecular receptors that feature curved concave surfaces complementary to the convex surface of fullerenes as a key recognizing element.
References
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Journal ArticleDOI

New Concepts in Tetrathiafulvalene Chemistry.

TL;DR: It has been confirmed that TTF can display efficient nonlinear optic responses in the second and third harmonic generation as well as a good thermal stability, which can be combined with the redox ability of TTF as an external stimuli to provide a promising strategy for the molecular engineering of switchable NLO materials.
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Multivalency and cooperativity in supramolecular chemistry.

TL;DR: This Account focuses on the application of multivalency to supramolecular chemistry in particular and the nanosciences in general.
Journal ArticleDOI

Positive allosteric systems designed on dynamic supramolecular scaffolds: toward switching and amplification of guest affinity and selectivity.

TL;DR: It has been suggested that positive homotropic allosterism can be utilized as a new strategy to attain high guest selectivity and guest affinity which cannot be attained by conventional 1:1-type guest binding.
Journal ArticleDOI

Molecular design of artificial molecular and ion recognition systems with allosteric guest responses.

TL;DR: In this Account, the basic concept for molecular design of such allosteric systems and what kinds of new functions come out of such dynamic systems are discussed.
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