Now, it is still a formidable challenge to design and synthesize solution-processable thermally activated delayedfluorescence (TADF) red emitters for organic light-emitting diodes (OLEDs). In this work, 1,8-naphthimide-9,9dimethyl-9,10-dihydroacridine units (NDMAC) and N,N-dicarbazolyl-3,5-benzene (mCP) units were bound to calix [4]resorcinarene (CRA) core to construct hyper-structured molecule (HSM) though two-step azide-alkyne "click" reaction. The HSMs, CRA-NDMAC(X)-mCP(100-X) (X = 0, 12.5, 25, 50, 75, 87.5, or 100), showed good solubilities, high thermal stabilities and good film-forming properties. Meanwhile, they also inherited the photophysical and electrochemical properties of the functional units due to the flexible inert linkage. The non-doped devices with spin-coating CRA-NDMAC(X)-mCP(100-X) as the emitting layer showed orange red to red emission with the peak wavelength from 600 nm to 630 nm. Among them, CRA-NDMAC(25)-mCP(75)-based device showed the maximum external quantum (EQEmax) of 1.6% with the peak wavelength at 612 nm, indicating that CRANDMAC(X)-mCP(100-X) could serve as a good candidate for solution-processable self-host TADF red emitter. More importantly, the design and synthesis strategy of CRA-NDMAC(X)-mCP(100-X) could provide a new simple strategy for the solution-processable TADF emitter.