Due to their outstanding and versatile properties, polybenzoxazines have quickly occupied a great niche of applications. Developing the ability to polymerize benzoxazine resin at lower temperatures than the current capability is essential in taking advantage of these exceptional properties and remains to be most challenging subject in the field. The current review is classified into several parts to achieve this goal. In this review, fundamentals on the synthesis and evolution of structure, which led to classification of PBz in different generations, are discussed. Classifications of PBzs are defined depending on building block as well as how structure is evolved and property obtained. Progress on the utility of biobased feedstocks from various bio-/waste-mass is also discussed and compared, wherever possible. The second part of review discusses the probable polymerization mechanism proposed for the ring-opening reactions. This is complementary to the third section, where the effect of catalysts/initiators has on triggering polymerization at low temperature is discussed extensively. The role of additional functionalities in influencing the temperature of polymerization is also discussed. There has been a shift in paradigm beyond the lowering of ring-opening polymerization (ROP) temperature and other areas of interest, such as adaptation of molecular functionality with simultaneous improvement of properties.

Exploring sustainable approaches to replace petroleum-based chemicals is an ongoing challenge in reducing the carbon footprint. Due to the complexity and percentage variation in nature-generated molecules, which further varies based on geographical origin and the purification protocol adopted, a better isolation strategy for individual components is required. Agrowaste from the cashew industry generates phenolic lipid (cardanol)-rich cashew nutshell liquid (CNSL) and has recently shown extensive commercial utility. Cardanol naturally exists as a mixture of three structurally different components with C₁₅-alkylene chains: monoene, diene, and triene. The separation of these three fractions has been a bottleneck and is crucial for certain structural designs and reproducibility. Herein, we describe the gram-scale purification of cardanol into each component using flash column chromatography within the sustainability framework. The solvent used for elution is recovered and reused after each stage (up to 82%), making it a cost-effective and sustainable purification strategy. This simple purification technique replaces the alternative high-temperature vacuum distillation, which requires substantial energy consumption and poses vacuum fluctuation and maintenance challenges. Three components (monoene 42%, diene 22%, and triene 36%) were isolated with good purity and were fully characterized by ¹H and ¹³C NMR, GC-MS, HPLC, and FTIR spectroscopy. The present work demonstrates that greener and simpler strategies pave the way for the isolation of constituents from nature-sourced biochemicals and unleash the potential of CNSL-derived fractions for high-end applications.