Understanding the dynamic processes
of CO
2
capture in
biosystems is important because of the great effect CO
2
has on the carbon cycle, human health, the global climate, and living
environments. After years of multidisciplinary studies, researchers
have gained only basic mechanistic knowledge about how enzymes or
protein-aggregates capture and deliver CO
2
, a process involving
reversible bonding of CO
2
with basic amino acid residues.
However, vital mechanistic details of how the activated basic residues
within these enzymes or protein-aggregates are initially formed, a
crucial step for CO
2
capture, are still lacking. Herein,
we designed specific molecules, i.e., oxazolidines, which are able
to reversibly change their alkalinity via ultrafast isomerizations.
Serving as so-called transient bases, these oxazolidines mimic the
activated/deactivated states of enzymes or protein-aggregates responsible
for dynamic CO
2
capture/release. A detailed mechanism for
CO
2
capture, which involves dynamic covalent bonding and
multimolecular cooperative interactions among functional groups that
occur with the help of a polyhydroxyl environment, is demonstrated
by UV−vis and multiple NMR spectroscopies as well as theoretical
calculations. Using suitable oxazolidine transient bases, applications
for visual CO
2
detection under different detection limit
requirements were also developed. Insights for further understanding
the process of dynamic CO
2
capture in biosystems are also
discussed. This oxazolidine-inspired biomimetic CO
2
capture
serves as a platform for the future development of additional biomimicking
systems, as well as offers unique perspectives for other complicated
life processes.