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October 6, 2015Angewandte Chemie International Edition224 citations

Unusual Aggregation‐Induced Emission of a Coumarin Derivative as a Result of the Restriction of an Intramolecular Twisting Motion

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FBFan BuRDRuihong DuanYXYujun Xie

Key Points

  • To elucidate the emission mechanism of a rotor-free coumarin derivative and determine how ring size and intramolecular motion govern aggregation-induced emission.
  • Synthesized a flexible seven-membered aliphatic ring coumarin derivative (CD-7) and a rigid five-membered analogue (CD-5).
  • Characterized fluorescence behavior in solution and aggregate states using experimental spectroscopy combined with theoretical calculations of excited-state twisting dynamics.
  • CD-7 exhibited aggregation-induced emission (AIE) due to aggregate-state restriction of out-of-plane backbone twisting that blocks rapid nonradiative decay, while CD-5 displayed aggregation-caused quenching (ACQ).
  • Modulating aliphatic ring size and molecular rigidity enabled direct switching between AIE and ACQ states without relying on conventional propeller-like aromatic rotor structures.

Abstract

Aggregation-induced emission (AIE) is commonly observed for propeller-like luminogens with aromatic rotors and stators. Herein, we report that a coumarin derivative containing a seven-membered aliphatic ring (CD-7) but no rotors showed typical AIE characteristics, whereas its analogue with a five-membered aliphatic ring (CD-5) exhibited an opposite aggregation-caused quenching (ACQ) effect. Experimental and theoretical results revealed that a large aliphatic ring in CD-7 weakens structural rigidity and promotes out-of-plane twisting of the molecular backbone to drastically accelerate nonradiative excited-state decay, thus resulting in poor emission in solution. The restriction of twisting motion in aggregates blocks the nonradiative decay channels and enables CD-7 to fluoresce strongly. The results also show that AIE is a general phenomenon and not peculiar to propeller-like molecules. The AIE and ACQ effects can be switched readily by the modulation of molecular rigidity.

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Cite This Study

Bu et al. (2015) studied this question.

synapsesocial.com/papers/6a1b5d11db618aee6aabcc46https://doi.org/10.1002/anie.201506782
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