The recovery of waste materials with potential for synthetic transformations is a major field in science. However, just few experiments have been devoted to undergraduate students by exploring some consistent subjects in light of simple, natural resources. Nucleophilicity is a central subject in chemistry and there are significant synthetic models to exploit it in contrast to basicity. Here we present a laboratory experiment that utilizes hands-on research to be implemented in an organic chemistry lab by using benzyl isothiocyanate (BITC) from papaya seeds as raw material for the preparation of thioureas in a fast and visually indicative experiment. Subjects such as green chemistry, extraction methods, nucleophilicity, chromatography and NMR spectroscopy can be emphasized in order to implement a project-based approach. This experiment shows flexibility concerning the procedures and the use of biomass raw materials towards the reinforcement of a research-like experience and critical-thinking skills.

A técnica de HPLC por troca de ligante foi utilizada para a separação de racematos de amino ácidos com cadeia lateral alifática. Para tanto, o seletor quiral escolhido foi o complexo de Cu(II) combinado com a L-fenilalananina. Os resultados mostram que o primeiro enanciômero a eluir foi a forma D, seguido da forma L. Segundo o conceito de interação de 3 pontos, foi proposto um mecanismo de reconhecimento quiral, no qual não há evidências de mudança de configuração após a formação dos complexos pseudo-homo e heteroquiral. Cálculos DFT-B3LYP para energia e espectro vibracional confirmaram a viabilidade deste mecanismo, pois mostram a que a configuração trans do complexo homoquiral é mais estável do que a forma cis.

Ligand exchange HPLC technique was applied to resolve chiral separation of aliphatic side chain aminoacid racemates. Chiral selector was copper L-phenylalaninate (II) and the results showed the elution of D enantiomer followed by L form. Considering the 3-point interaction concept, a mechanism of chiral recognition was proposed, in which no change of configuration would follow the formation of pseudo-homochiral and heterochiral complexes. To prove the reliability of this mechanism, the trans configuration of homochiral complex had to be more stable than the cis form, which was confirmed by DFT-B3LYP calculation in gas phase. The infrared frequencies were also calculated and the comparison with the subtracted and deconvoluted spectrum of the in-solution complex also pointed to the presence of the trans diasteroisomer.