A series of fully conjugated graft copolymers containing poly(3-hexylthiophene) (P3HT) side chains and a p-type carbazole-diketopyrrolopyrrole (CbzDPP) donor-acceptor backbone were synthesized via a graft through Suzuki polymerization. The macromonomers were formed by externally initiating P3HT growth from a boronic ester-functionalized carbazole via Kumada catalyst transfer polycondensation. Subsequently, this macromonomer was copolymerized with a DPP monomer via a graft through Suzuki polymerization to yield the final graft copolymers. The graft copolymers exhibit optical and electronic properties of both P3HT and the CbzDPP polymers independently due to the break in conjugation between the carbazole unit and P3HT chain. Moreover, these properties reflect the relative proportion of P3HT and CbzDPP polymers; shorter P3HT chain lengths lead to graft copolymers that possess more CbzDPP character and vice versa. The macromonomers were characterized by gel permeation chromatography, mass spectrometry, and UV-visible spectroscopy. The graft copolymers were further investigated using gel permeation chromatography, UV visible spectroscopy, cyclic voltammetry, differential scanning calorimetry, and atomic force microscopy. Finally, organic field effect transistors were fabricated using the graft copolymers and compared to an analogous linear CbzDPP copolymer. Ultimately, the graft copolymers with the longest P3HT chains (ca. 75 repeat units) exhibited almost exclusively P3HT characteristics, possessing a small CbzDPP internal charge transfer (ICT) peak and only p-type conductivity (mu(h) similar to 6 X 10(-4) cm(2) V-1 s(-1)). Conversely, the graft copolymers with the shortest P3HT chains (ca. 10 repeat units) showed significant CbzDPP character, including a strong ICT peak and ambipolar mobilities (mu(h) similar to 5 X 10(-3) cm(2) V-1 s(-1); mu(e) similar to 7 X 10(-4) cm(2) V-1 s(-1)).