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Triplet States of Cyanostar and Its Anion Complexes

Edhborg, Fredrik, 1990 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Olesund, Axel, 1990 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Tripathy, Vikrant (author)
Indiana University
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Wang, Yang (author)
Köpenhamns universitet,University of Copenhagen
Sadhukhan, Tumpa (author)
SRM Institute of Science and Technology,Indiana University
Olsson, Andrew H. (author)
Indiana University
Bisballe, Niels (author)
Köpenhamns universitet,University of Copenhagen
Raghavachari, Krishnan (author)
Indiana University
Laursen, Bo W. (author)
Köpenhamns universitet,University of Copenhagen
Albinsson, Bo, 1963 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Flood, Amar H. (author)
Indiana University
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 (creator_code:org_t)
2023
2023
English.
In: Journal of Physical Chemistry A. - 1089-5639 .- 1520-5215. ; 127:28, s. 5841-5850
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The design of advanced optical materials based on triplet states requires knowledge of the triplet energies of the molecular building blocks. To this end, we report the triplet energy of cyanostar (CS) macrocycles, which are the key structure-directing units of small-molecule ionic isolation lattices (SMILES) that have emerged as programmable optical materials. Cyanostar is a cyclic pentamer of covalently linked cyanostilbene units that form π-stacked dimers when binding anions as 2:1 complexes. The triplet energies, ET, of the parent cyanostar and its 2:1 complex around PF6- are measured to be 1.96 and 2.02 eV, respectively, using phosphorescence quenching studies at room temperature. The similarity of these triplet energies suggests that anion complexation leaves the triplet energy relatively unchanged. Similar energies (2.0 and 1.98 eV, respectively) were also obtained from phosphorescence spectra of the iodinated form, I-CS, and of complexes formed with PF6- and IO4- recorded at 85 K in an organic glass. Thus, measures of the triplet energies likely reflect geometries close to those of the ground state either directly by triplet energy transfer to the ground state or indirectly by using frozen media to inhibit relaxation. Density functional theory (DFT) and time-dependent DFT were undertaken on a cyanostar analogue, CSH, to examine the triplet state. The triplet excitation localizes on a single olefin whether in the single cyanostar or its π-stacked dimer. Restriction of the geometrical changes by forming either a dimer of macrocycles, (CSH)2, or a complex, (CSH)2·PF6-, reduces the relaxation resulting in an adiabatic energy of the triplet state of 2.0 eV. This structural constraint is also expected for solid-state SMILES materials. The obtained T1 energy of 2.0 eV is a key guide line for the design of SMILES materials for the manipulation of triplet excitons by triplet state engineering in the future.

Subject headings

NATURVETENSKAP  -- Kemi -- Oorganisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi -- Materialkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Materials Chemistry (hsv//eng)

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