Chiral SiO 2 nanofibers associated with polyamines on their surfaces could promote polymerization between resorcinol and formaldehyde on silica surface to give phenolic resins (RF). In this process, the chiral information was effectively transferred from SiO 2 to the final phenolic resins forming double chiral hybrid.Keywords: Double chiral hybrid | Chiral SiO 2 nanofiber | Chiral phenolic resinThe synthesis of chiral polymers with optical activity is of major importance because of their great demand in many areas like life sciences, pharmaceuticals, and optics.13 To achieve chirality in polymers during the polymerization process, various chiral sources have been employed for chiral transfer, which includes chiral organometallic complexes catalysts, chiral organic solvents, chiral polymeric templates, and even circular polarized light.4 On the other hand, some inorganic materials (e.g., porous SiO 2 , metal nanoparticles) have been widely used as supports for the load of chiral components to construct various heterogeneous catalysts, which possess advantages like easy separation and recycling of catalysts; however, most of these inorganic supports are achiral. 57 Based on the best of our understanding, to date, there are no reports on chiral polymerization using achiral catalyst supported by chiral inorganic supports.For a long time, the chiral inorganics are less of a concern compared with organics, despite the existence of natural inorganic crystals with intrinsically chiral crystal structures (e.g., quartz) or surfaces (e.g., Pt(643)). 8,9 However, in the past two decades, the research on the chiral transfer between organics and inorganics has gained increasing attention, and a series of synthetic inorganics have been endowed with chirality by molecular imprinting from small chiral organic molecules (on the molecular scale) or by copying the helical shapes (with helical pitch sizes over tens of nanometers) of organic templates.10,11 Interestingly, without the combination of external chiral components, it has been demonstrated that some natural and synthetic chiral inorganics could be directly applied to the enantioselective separation and synthesis of chiral organic small molecules (e.g., amino acids, glucoses).9,1215 Consequently, these achievements have opened a new avenue for chirality transfer from inorganics to organics. Recently, we reported a successful approach for the preparation of carbon nanotubes via carbonization of hybrid nanofibers of phenolic resins-coated silica which were synthesized by polymerization of resorcinol and formaldehyde on the polyamine (catalyst)-associated silica (template and support) nanofibers. 16 On the other hand, we also succeeded in the synthesis of chiral silica promoted by crystalline complexes self-assembled from polyethyleneimine (PEI) and enantiomeric tartaric acid (tart).17 By combining the above two achievements, herein, we attempted the synthesis of chiral phenolic resins (RF) by polymerization of resorcinol (R) and formaldehyde (F), employing the SiO 2 /PEI chi...