In this paper, a brief review of the syntheses, characterization and anion-binding properties of core-modified octaphyrins is presented. It has been shown that the core-modified octaphyrins exhibit aromaticity both in solution and in solid state, confirming the validity of the (4n + 2) Huckel rule for larger π-electron systems. Solid-state binding characteristics of TFA anions of two core-modified octaphyrins are also described
Metalloporphyrins and related macrocycles have been of great interest due to their role in biology a...
Porphyrins are tetrapyrrolic 18 π electron conjugated macrocycles with wide applications that r...
Chapter 1 introduces the N?H?X binding motif in tetrapyrroles, which forms the basis of the research...
In this paper, a brief review of the syntheses, characterization and anion-binding properties of cor...
Modified octaphyrins with 34π electrons have been synthesized and characterized following a sim...
The synthesis and structural characterization of the first examples of aromatic core-modified figure...
Successful syntheses of two new aromatic core modified oxybenziporphyrins by a simple 3 + 1 methodol...
Modified 26π rubyrin, 36π octaphyrin, and 54π dodecaphyrin systems have been synthesi...
Expanded porphyrins containing seven pyrrole/heterocyclic rings linked in a cyclic fashion are terme...
Proton-coupled electron transfer (PCET) is an important chemical and biological phenomenon. It is at...
Proton-coupled electron transfer (PCET) is an important chemical and biological phenomenon. It is at...
Proton-coupled electron transfer (PCET) is an important chemical and biological phenomenon. It is at...
Synthesis and characterization of several 26π core-modified hexaphyrins are reported. The synth...
Over the last two decades the preparation of pyrrole-based receptors for anion recognition has attra...
The thesis proposes to refine and extend the ‘porphyrin breaking and mending’ methodology, to modify...
Metalloporphyrins and related macrocycles have been of great interest due to their role in biology a...
Porphyrins are tetrapyrrolic 18 π electron conjugated macrocycles with wide applications that r...
Chapter 1 introduces the N?H?X binding motif in tetrapyrroles, which forms the basis of the research...
In this paper, a brief review of the syntheses, characterization and anion-binding properties of cor...
Modified octaphyrins with 34π electrons have been synthesized and characterized following a sim...
The synthesis and structural characterization of the first examples of aromatic core-modified figure...
Successful syntheses of two new aromatic core modified oxybenziporphyrins by a simple 3 + 1 methodol...
Modified 26π rubyrin, 36π octaphyrin, and 54π dodecaphyrin systems have been synthesi...
Expanded porphyrins containing seven pyrrole/heterocyclic rings linked in a cyclic fashion are terme...
Proton-coupled electron transfer (PCET) is an important chemical and biological phenomenon. It is at...
Proton-coupled electron transfer (PCET) is an important chemical and biological phenomenon. It is at...
Proton-coupled electron transfer (PCET) is an important chemical and biological phenomenon. It is at...
Synthesis and characterization of several 26π core-modified hexaphyrins are reported. The synth...
Over the last two decades the preparation of pyrrole-based receptors for anion recognition has attra...
The thesis proposes to refine and extend the ‘porphyrin breaking and mending’ methodology, to modify...
Metalloporphyrins and related macrocycles have been of great interest due to their role in biology a...
Porphyrins are tetrapyrrolic 18 π electron conjugated macrocycles with wide applications that r...
Chapter 1 introduces the N?H?X binding motif in tetrapyrroles, which forms the basis of the research...