TY - UNPB
T1 - Inducing Social Self-Sorting in Organic Cages to Tune the Shape of the Internal Cavity
AU - Abet, Valentina
AU - Szczypiński, Filip T.
AU - Little, Marc A.
AU - Santolini, Valentina
AU - Jones, Christopher D.
AU - Evans, Robert
AU - Wilson, Craig
AU - Wu, Xiaofeng
AU - Thorne, Michael F.
AU - Bennison, Michael J.
AU - Cui, Peng
AU - Cooper, Andrew I.
AU - Jelfs, Kim E.
AU - Slater, Anna G.
N1 - CC BY-NC-ND 4.0
Funding: EP/R005931/1
EP/L000202
EP/R029431
EP/N004884/1
CY21726
Leverhulme Trust Research Project Grant
Royal Society-EPSRC Dorothy Hodgkin Fellowship
Royal Society University Research Fellowship
PY - 2020/5/26
Y1 - 2020/5/26
N2 - Many interesting target guest molecules have low symmetry, yet most methods for synthesising hosts result in highly symmetrical capsules. Methods of generating lower-symmetry pores are thus required to maximise the binding affinity in host-guest complexes. Here, we use mixtures of tetraaldehyde building blocks to access low-symmetry imine cages. Whether a low-energy cage is isolated can be correctly predicted from the thermodynamic preference observed in computational models. The stability of the observed structures depends on the geometrical match of the aldehyde building blocks. One bent aldehyde stands out as unable to assemble into high-symmetry cages—and the same aldehyde generates low-symmetry socially self-sorted cages when combined with a linear aldehyde. We exploit this finding to synthesise a family of low-symmetry cages containing heteroatoms, illustrating that pores of varying geometries and surface chemistries may be reliably accessed through computational prediction and self-sorting.
AB - Many interesting target guest molecules have low symmetry, yet most methods for synthesising hosts result in highly symmetrical capsules. Methods of generating lower-symmetry pores are thus required to maximise the binding affinity in host-guest complexes. Here, we use mixtures of tetraaldehyde building blocks to access low-symmetry imine cages. Whether a low-energy cage is isolated can be correctly predicted from the thermodynamic preference observed in computational models. The stability of the observed structures depends on the geometrical match of the aldehyde building blocks. One bent aldehyde stands out as unable to assemble into high-symmetry cages—and the same aldehyde generates low-symmetry socially self-sorted cages when combined with a linear aldehyde. We exploit this finding to synthesise a family of low-symmetry cages containing heteroatoms, illustrating that pores of varying geometries and surface chemistries may be reliably accessed through computational prediction and self-sorting.
M3 - Working paper
BT - Inducing Social Self-Sorting in Organic Cages to Tune the Shape of the Internal Cavity
ER -