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Ultrafast Excited State Dynamics in Twisted Aromatics

סמינר כימיה פיזקאלית ואנאליטית

מרצה: Prof. Mahesh Hariharan

תאריך:
14-14 Apr 2019 @ 12:30

מיקום: חדר סמינרים פקולטי

Ultrafast Excited State Dynamics in Twisted Aromatics

Molecules that produce charges when excited by light are useful for a variety of (bio-) organic electronic applications. To maximize the utility of these molecules, researchers work to keep the induced charges separate for as long as possible. Stacking the excitable molecules can extend the charge lifetime, but often the donor and acceptor parts of the molecule naturally alternate in the stack, which causes the charges to immediately recombine. Our group aim to minimize charge recombination[1-5] by separating the donor and acceptor portions of the molecule on different spatial planes. We have synthesized a naphthalimide-naphthalene dyad where the donor and acceptor units are twisted into different planes. The twisted monomers also assemble into a stacked tower. When illuminated by UV light, the charge separated state of the stack can last more than 1.2 ns, 10,000 times longer than in the monomeric dyad (Scheme 1). This assembly could be a novel scaffold for light harvesting, molecular electronics, or new light-induced electronic applications. As opposed to the conventional view of modulating the redox properties and/or distance between donor and acceptor, our results encourage to focus on fine-tuning of spatial organisation of the donor and acceptor chromophores to hop the charges over long distances.

Scheme 1. Representative strategies adopted in our group to spatially organize electron donors and acceptors for emergent properties.

[1]    a) M. Hariharan et al., J. Am. Chem. Soc., 137, 15604 (2015). b)  M. Hariharan et al., J. Phys. Lett., 7, 4751 (2016). c) M. Hariharan et al., Chem. Sci., 8, 1776 (2017). d) M. Hariharan et al., Chem. Eur. J., 24, 12318 (2018) e) M. Hariharan et al., Chem. Eur. J., 24, 8679 (2018). f) M. Hariharan et al., Angew. Chem. Int. Ed., 57, 15696 (2018).

[2]      M. Hariharan et al., Energy Environ. Sci., 7, 1661 (2014).

[3]      M. Hariharan et al., J. Phys. Chem. C, 117, 3240 (2013).

[4]      M. Hariharan et al., J. Phys. Chem. C, 116, 12489 (2012).

[5]      a) M. Hariharan et al., J. Phys. Chem. C, 121, 4778–4788 (2017). b) M. Hariharan et al., J. Phys. Chem. C, 121, 4765–4777 (2017). c) M. Hariharan et al., J. Phys. Chem. C, 121, 23259-23267 (2017).