Novel bacteriochlorophyll-d analogs demonstrate self-aggregation in alkanes, suggesting design impacts on stability.
Novel bacteriochlorophyll-d analogs bearing a highly hydrophobic Polyhedral Oligomeric SilSesquioxane (POSS) unit linked by an ester or an amide bond on the 17-position were synthesized, and their chlorosomal self-aggregation behavior was demonstrated in single-alkane solvents. Both derivatives formed J-aggregates after refluxing in neat n-decane, similar to those obtained in tetrahydrofuran–n-hexane mixed-solvent systems. Temperature-dependent measurements revealed superior thermal stability for the amide-type analog, highlighting the crucial role of the 17-substituent design in controlling chlorosomal self-aggregation.
No takes yet. Share an insight, caveat, or question.
Shoji et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: