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Updated: Feb 11, 2026

Negative Additive Manufacturing of Complex Shaped Boron Carbides
Published on: September 18, 2018
A Boron-Bridged Tetrathiaporphyrinogen.
Francis H Carré1, Robert J-P Corriu1, Thomas Deforth1
1CNRS UMR 5637, Université Montpellier II, Place E. Bataillon, F-34095 Montpellier cedex 5 (France), Fax: (+33) 467143888.
Researchers synthesized a novel boron-bridged thiophene-containing porphyrinogen with simultaneous Lewis acid and base centers. Its nonplanar structure and colorless nature indicate a lack of delocalized pi-electron systems, impacting its electronic properties.
Area of Science:
- Supramolecular Chemistry
- Organic Synthesis
- Materials Science
Background:
- Porphyrinogens are macrocyclic compounds with diverse applications.
- Understanding the structure-property relationships of novel porphyrinogen derivatives is crucial for developing new materials.
Purpose of the Study:
- To synthesize and characterize a novel boron-bridged thiophene-containing porphyrinogen.
- To investigate the structural and electronic properties of the synthesized compound.
Main Methods:
- High-yield synthesis of the target porphyrinogen.
- Single-crystal X-ray diffraction analysis to determine the molecular structure.
- Spectroscopic analysis to probe electronic properties.
Main Results:
- Successful synthesis of boron-bridged thiophene-containing porphyrinogen 1 in high yield.
- Crystal structure revealed a nonplanar macrocyclic structure.
- The compound's colorless appearance and nonplanar geometry suggest the absence of a delocalized pi-electron system.
Conclusions:
- The synthesized porphyrinogen possesses both Lewis acid and Lewis base centers.
- The nonplanar macrocycle and lack of delocalized pi-electrons influence its electronic behavior.
- This compound represents a unique structural motif for potential applications in catalysis or materials science.
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