A series of novel hybrids of artemisinin (ART) with either a phytormone endoperoxide G factor analogue (GMeP) or chloroquine (CQ) and conjugates of the same compounds with the polyamines (PAs), spermidine (Spd), and homospermidine (Hsd) were synthesized and their antiplasmodial activity was evaluated using the CQ-resistant P. falciparum FcB1/Colombia strain. The ART-GMeP hybrid 5 and compounds 9 and 10 which are conjugates of Spd and Hsd with two molecules of ART and one molecule of GMeP, were the most potent with IC₅₀ values of 2.6, 8.4, and 10.6 nM, respectively. The same compounds also presented the highest selectivity indexes against the primary human fibroblast cell line AB943 ranging from 16 372 for the hybrid 5 to 983 for the conjugate 10 of Hsd.

There are few examples of covalent organic frameworks (COFs) based on phosphorus as the building element, probably because the structure of most phosphorus derivatives is pyramidal, which may prevent the stacking expected for classical 2-dimensional COFs. In addition, they are generally associated with linear difunctional derivatives. In this paper is reported the original association of a trifunctional 3-D compound with a trifunctional 2-D compound in an attempt to get a new COF. The condensation reaction between a thiophosphate derivative bearing three aldehydes and the trihydrazinotriazine has been carried out with the aim of obtaining either a COF or simply a porous organic polymer (POP), consisting in both cases of associated macrocycles, affording a new covalent triazine framework (CTF). The material resulting from this condensation has been characterized by multinuclear MAS NMR (³¹P, ¹H, and ¹³C), IR, and thermogravimetric analysis (TGA). All these data confirmed the condensation reactions. However, BET (Brunauer–Emmett–Teller) measurements indicated that the porosity of this material is low. Trapping dyes in solution, as a model of pollutants, by the insoluble porous material 3 has been attempted.