Article ID Journal Published Year Pages File Type
5411976 Journal of Molecular Liquids 2013 15 Pages PDF
Abstract

•Synthesis of new dendrimers•Physicochemical properties with DMSO•Alkyl chain activities•Molecular interaction•Thermal behaviour

Trimesoyl 1, 3, 5-tridimethyl malonate (TTDMM) and trimesoyl 1, 3, 5-tridiethyl malonate (TTDEM) dendrimers synthesised from trimesoyl chloride (TMC) with dialkyl malonate ester (DME) in 1:3 mass ratio in alcoholic medium are reported. TTDMM and TTDEM as white solids with ≈ 95% yield have shown 144.22 °C and 131.78 °C MP respectively. FTIR and 500 MHz 1H NMR have determined structures and thermal stability was studied with DSC. Their densities (ρ ± 103 kg m− 3), viscosities (η ± 10− 4 mPa·s), surface tension (γ ± 0.01 mN m− 1) and activation energies (Δμ2* ± 10− 2 kJ/mol) for 2.0 to 8.0 mM/L were determined with DMSO at 298.15 K. Activation energies were calculated from viscosities. Data were regressed for limiting densities, viscosities, surface tension and activation energies for dendrimer-DMSO interaction activities. Negative limiting activation energy values (Δμ2* < 0) as TTDMM > TTDEM inferred comparatively higher energy utilization with ethyl group. Higher limiting density and viscosity for TTDEM have depicted stronger TTDEM-DMSO interaction due to higher entanglement with stronger structural activities as compared to TTDMM. This paper focuses on the role of CH2 of dialkyl malonate ester on their structural and physicochemical properties for using these dendrimers as drug vehicles.

Related Topics
Physical Sciences and Engineering Chemistry Physical and Theoretical Chemistry
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