a b s t r a c t A series of novel brush triblock copolymers containing 'glassy' fluorinated polyimide, poly((4,4 0 -hexa-fluoroisopropylidene diphthalic anhydride)-co-(2,3,5,6-tetramethyl-1,4-phenylenediamine)) (poly(6FDA-co-TMPD)), and 'rubbery' polydimethylsiloxane monomethacrylate (PDMS-MA) were synthesized and characterized. Well-defined difunctional poly(6FDA-co-TMPD) with a,u-amino end-groups was initially prepared via step-growth polymerization using precise control of the diamine (TMPD) to dianhydride (6FDA) ratio. Subsequent functionalization with 2-bromoisobutyryl bromide afforded a telechelic mac-roinitiator suitable for atom transfer radical polymerization (ATRP). The macroinitiator and its diamino poly(6FDA-co-TMPD) precursor were characterized via gel permeation chromatography (GPC), 1 H nuclear magnetic resonance (NMR) spectroscopic analysis and matrix assisted laser desorption ionization time-of-flight (MALDI ToF) mass spectroscopy. ATRP of PDMS-MA using the macroinitiator in different molar ratios afforded a series of brush triblock copolymers with high monomer conversions (88e94%) and varying PDMS weight fractions. Self-assembly of the triblock brush copolymers in dimethylformamide (DMF) afforded nanoparticles with hydrodynamic diameters (d H) ranging from 87 to 109 nm, as deter-mined by dynamic light scattering (DLS) analysis. Cross-linking of the nanoparticles was achieved via hydrogen abstraction through the thermal degradation of benzoyl peroxide. Transmission electron microscopy (TEM) and scanning transmission electron microscopy (STEM) revealed that the self-assemblies and their cross-linked derivatives had spherical morphologies.