AI Article Synopsis

  • The study focuses on creating fullerene derivatives that can have their polarities adjusted, ranging from superhydrophobic to hydrophilic, to enhance their reactivity and potential for further applications.
  • The synthesis process involves using an isoxazoline moiety for selective protection, resulting in mixed hexakisadducts that provide desired solubility properties.
  • The resultant fullerene derivatives have been characterized for their hydrophobic/hydrophilic behavior and can form supramolecular structures, which were analyzed using techniques like dynamic light scattering and cryo-TEM.

Article Abstract

Herein, the synthesis of fullerene derivatives with adjustable polarities and lyotropic aggregation properties is reported. The polarity range spans from superhydrophobic to hydrophilic, while simultaneously providing a further reactive position with a view to graft them onto other materials. The synthetic strategy relies on a selective protection with an isoxazoline moiety. The remaining octahedral positions were further functionalized with the desired groups to tune their solubility, yielding mixed [5:1] hexakisadducts. The subsequent deprotection by clean photolytic reaction led to fullerene pentakisadducts with an incomplete octahedral addition pattern, which are useful forerunners for the synthesis of building blocks. Their hydrophobic/hydrophilic behavior has been characterized both in solution and surface through octanol/water partition coefficients (log P) and contact angle measurements. Furthermore, these derivatives can form supramolecular constructions which have been studied by dynamic light scattering (DLS) and cryo-TEM.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585616PMC
http://dx.doi.org/10.1002/chem.201803036DOI Listing

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