Electrophilic iodination of thiophene and its electron‐poor derivatives has been studied with KICl2in dichloromethane and methanol using density function theory. KICl2easily dissociates forming KCl and ICl, the latter being the iodinating agent. ICl forms an adduct with thiophene (π‐complex) followed by a nucleophilic attack of the ICl component by the aromatic component that forms the C–I bond. The nucleophilic attack is always the rate determining step with higher barriers that are in agreement the experimental conditions required for this reaction. The abstraction of a proton by the chloride anion on the last step is barrierless leading to the mono‐ and di‐iodination of the thiophene derivatives. Side products derived from the nucleophilic addition of the chloride anion have been determined to be transient.
This content will become publicly available on July 30, 2025
The incorporation of cationic groups onto electron‐poor compounds is a viable strategy for achieving potent electron acceptors, as evidenced by reports of air‐stable radical forms of large aromatic diimides such as naphthalene and perylene diimides. These ions have also been observed to exhibit anion–π interaction tendencies of interest in molecular recognition applications. The benefits of phosphonium incorporation, however, have not yet been extended to the smallest benzene diimides. Here, we report that dibrominated pyromellitic diimide and mellophanic diimide both readily undergo substitution reactions with phosphine sources to yield bisphosphonium compounds. In the single crystalline form, these dications display anion‐π interactions and, in the case of mellophanic diimide, the stabilization of a bromide–water H−bonding ring pattern. The reaction of these dications with chemical reductants readily provides the singly and doubly reduced redox states, which were characterized by UV‐vis spectroscopy and found to exhibit intense absorptions extending into the near‐IR region. Taken together, this work demonstrates that phosphonium incorporation onto congested aromatic diimide scaffolds is synthetically viable and produces unusual electron‐poor compounds.
more » « less- PAR ID:
- 10550116
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Chemistry – A European Journal
- Volume:
- 30
- Issue:
- 57
- ISSN:
- 0947-6539
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
more » « less
Abstract -
more » « less
Abstract A new approach to fused helicenes is reported, where varied substituents are readily incorporated in the extended aromatic frame. From the alkynyl precursor, the final helical compounds are obtained under mild conditions in a two‐step process, in which the final C−C bond is formed via a photochemical cyclization/ dehydroiodination sequence. The distortion of the π‐system from planarity leads to unusual packing in the solid state. Computational analysis reveals that substituent incorporation perturbs geometries and electronic structures of these nonplanar aromatics.
-
more » « less
Abstract With the view of developing selective transmembrane anion transporters, a series of phosphonium boranes of general formula [
p ‐RPh2P(C6H4)BMes2]+have been synthesized and evaluated. The results demonstrate that variation of the R group appended to the phosphorus atom informs the lipophilicity of these compounds, their Lewis acidity, as well as their transport activity. Anion transport experiments in POPC‐based large unilamellar vesicles show that these main‐group cations are highly selective for the fluoride anion, which is transported more than 20 times faster than the chloride anion. Finally, this work shows that the anion transport properties of these compounds are extremely sensitive to the steric crowding about the boron atom, pointing to the crucial involvement of the Group 13 element as the anion binding site. -
more » « less
Abstract With the view of developing selective transmembrane anion transporters, a series of phosphonium boranes of general formula [
p ‐RPh2P(C6H4)BMes2]+have been synthesized and evaluated. The results demonstrate that variation of the R group appended to the phosphorus atom informs the lipophilicity of these compounds, their Lewis acidity, as well as their transport activity. Anion transport experiments in POPC‐based large unilamellar vesicles show that these main‐group cations are highly selective for the fluoride anion, which is transported more than 20 times faster than the chloride anion. Finally, this work shows that the anion transport properties of these compounds are extremely sensitive to the steric crowding about the boron atom, pointing to the crucial involvement of the Group 13 element as the anion binding site. -
Herein, we communicate that altering the number of carbon atoms on the alkoxyphenyl substituent in naphthalene diimides results in tunable thermo-salient behavior across a variety of temperatures. Additionally, these compounds were found to display reversible thermochromic behavior in the single crystalline state. We analyzed this behavior using differential scanning calorimetry (DSC), single crystal X-ray diffraction (SXRD), powder XRD (PXRD), and hot-stage microscopy. The heptoxyphenyl-, octoxyphenyl-, and nonoxyphenyl-derivatives exhibited “acrobatic” behavior—namely, bending, jumping, and splitting—upon an irreversible phase transition. This study contributes to a developing paradigm in the understanding of certain naphthalene diimide single crystals that the energy associated with irreversible phase transitions has the potential to perform mechanical work, and that the temperature at which this energy can be fine-tuned by selecting an appropriate alkoxyphenyl substituent. Furthermore, we show that these thermochromic NDI derivatives can be incorporated into commercially-available, polymeric 3D printing materials and the resulting printed mixed polymer-crystalline objects still exhibit thermochromic behavior after incorporation.more » « less
