Herein, we report copolymerizations of ethylene (E) and ortho-/meta-/para-fluorostyrenes (SF =oFS/mFS/pFS) by using quinolyl methylene fluorenyl scandium complex (Flu-CH2 -Qu)Sc(CH2 SiMe3 )2 . The copolymerizations proceed in a controlled fashion to afford copolymers composed of "soft" ethylene-fluorostyurene (E-SF ) random segments (Tg =-22.2-5.1 °C) and "hard" crystalline ethylene-ethylene (E-E) segments (Tm =42.3-130.2 °C). The copolymers behave like thermoplastic elastomers at room temperature by showing high stress values up to 39.5 MPa under elongation-at-break above 774 % with elastic recovery over 75 %. The excellent mechanical properties are mainly attributed to the microphase separation of the nanoscale crystalline E-E domain from the amorphous E-SF copolymer matrix proved by AFM, WAXD and SAXS. The mechanism investigation by the density functional theory (DFT) simulation reveals that the steric bulky and electron-withdrawing ligand of the catalytic precursor prefers E propagation to generate long E-E segments, while the incorporation of SF is thermodynamic control.