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Phosphorescent cocrystals constructed by 1,4-diiodotetrafluorobenzene and polyaromatic hydrocarbons based on C-I π halogen bonding and other assisting weak interactionsElectronic supplementary information (ESI) available: ATR-IR, Raman spectra and XRPD patterns. CCDC reference numbers 870890-870892. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ce25338k
The cocrystals were assembled with 1,4-diiodotetrafluorobenzene (1,4-DITFB) as the halogen bonding donor and the polycyclic aromatic hydrocarbons (PAH), biphenyl (Bp), naphthalene (Nap), phenanthrene (Phe), as the π-type halogen bonding acceptors, corresponding to cocrystals 3 (Bp-DITFB), 4 (Nap-DIT...
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Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | The cocrystals were assembled with 1,4-diiodotetrafluorobenzene (1,4-DITFB) as the halogen bonding donor and the polycyclic aromatic hydrocarbons (PAH), biphenyl (Bp), naphthalene (Nap), phenanthrene (Phe), as the π-type halogen bonding acceptors, corresponding to cocrystals
3
(Bp-DITFB),
4
(Nap-DITFB) and
5
(Phe-DITFB), respectively. The single crystal X-ray diffraction analysis reveals that the two-dimensional layer in
3
or the one-dimensional chain structures in
4
and
5
are formed by C-I π halogen bonds, and that the C-I π bonding occurs in both above-the-carbon and above-the-bond models of DITFB to PAHs. Other intermolecular interactions in cocrystals such as C-F F-C contacts, edge-to-edge type π-π stacking and C-H I hydrogen bonding are also significant in maintaining the stability of supramolecular structures. The stoichiometry of all three cocrystals is 1 : 2 of PAH to DITFB. The PAHs with smaller conjugation systems and linear (not more than two benzene rings) or bent structures may be apt to form cocrystals with 1,4-DITFB by C-I π halogen bonding. The cocrystals are well characterized by various spectroscopic methods. Additionally, the cocrystals
4
and
5
, as expected, produce strong green and orange phosphorescence, respectively, due to strong spin-orbital coupling of iodine atoms. Phosphorescence of Phe in cocrystal
5
appears to be largely red-shifted compared with regular emission in solution or on general solid-supports. The phosphorescence decay of cocrystals
4
and
5
both obey a mono-exponential form with lifetimes of 0.067 ms and 1.449 ms, respectively.
Phosphorescent cocrystals are assembled based on C-I π halogen bonding and the luminescence wavelength of phenanthrene is largely modulated in the cocrystal. |
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ISSN: | 1466-8033 |
DOI: | 10.1039/c2ce25338k |