Bipolaron

Bipolaron can have two different meanings, it can be a type of quasiparticle, or in organic chemistry it is either a molecule, or part of a macromolecular chain.

Bipolarons in physics

In physics, a bipolaron is a bound pair of two polarons. An electron in a material may cause a distortion in the underlying lattice. The combination of electron and distortion (which may also be understood as a cloud of phonons) is known as a polaron (in part because the interaction between electron and lattice is via a polarization). When two polarons are close together, they can lower their energy by sharing the same distortions, which leads to an effective attraction between the polarons. If the interaction is sufficiently large, then that attraction leads to a bound bipolaron. For strong attraction, bipolarons may be small. Small bipolarons have integer spin and thus share some of the properties of bosons. If many bipolarons form without coming too close, they might be able to form a Bose–Einstein condensate. This has led to a suggestion that bipolarons could be a possible mechanism for high temperature superconductivity. For example, they can lead to a very direct interpretation of the isotope effect.

Bipolarons in organic chemistry

In organic chemistry a bipolaron is a molecule or part of a macromolecular chain containing two positive charges in a conjugated system. The charges can be located in the centre of the chain or at its termini. Bipolarons and polarons are encountered in doped conducting polymers such as polythiophene.

It is possible to synthesize and isolate bipolaron model compounds for X-ray diffraction studies.[1] The diamagnetic bis(triaryl)amine dication 2 in scheme 1 is prepared from the neutral precursor 1 in dichloromethane by reaction with 4 equivalents of antimony pentachloride. Two resonance structures exist for the dication. Structure 2a is a (singlet) diradical and 2b is the closed shell quinoid. The experimental bond lengths for the central vinylidene group in 2 are 141 pm and 137 pm compared to 144 pm and 134 pm for the precursor 1 implying some contribution from the quinoid structure.

On the other hand when a thiophene unit is added to the core in the structure depicted in scheme 2, these bond lengths are identical (around 138 pm) making it a true hybrid.

See also

References

  1. ↑ S. Zheng; et al. (2006). "Isolation and Crystal Structures of Two Singlet Bis(Triarylamine) Dications with Nonquinoidal Geometries". Journal of the American Chemical Society 128 (6): 1812–7. doi:10.1021/ja0541534. PMID 16464079.
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