Investigating identification disparities in forensic anthropology casework.

Forensic anthropology is shifting to reflect on the impact of its practices within the criminal justice context in important ways. Here, we contribute to this essential work by examining how decedent demographics as well as estimations of biological profile components are related to identification trends in forensic anthropology cases. The study uses data from more than 1,200 identified and unidentified forensic anthropology cases from three agencies (together representing a nation-wide sample).

Synthesis and characterization of a block copolymer containing regioregular poly(3-hexylthiophene) and poly(γ-benzyl-L-glutamate).

Poly(3-hexylthiophene)-b-poly(γ-benzyl-L-glutamate) (P3HT-b-PBLG) rod-rod diblock copolymer was synthesized by a ring-opening polymerization of γ-benzyl-L-glutamate-N-carboxyanhydride using a benzylamine-terminated regioregular P3HT macroinitiator. The opto-electronic properties of the diblock copolymer have been investigated. The P3HT precursor and the P3HT-b-PBLG have similar UV-Vis spectra both in solution and solid state, indicating that the presence of PBLG block does not decrease the effective conjugation length of the semiconducting polythiophene segment.

Polymers containing rigid benzodithiophene repeating unit with extended electron delocalization.

Polymers containing a fused benzodithiophene core with phenylethynyl substituents were prepared. The parent poly[4,8-bis(4-pentylphenylethynyl)benzo[1,2-b:4,5-b']dithiophene] was prepared by a Stille coupling. Copolymers with the new core were also obtained by Stille coupling with dibrominated fluorene and carbazole monomers.