Isolation and characterization of homoisoflavonoids from Scilla persica HAUSSKN

Plantas medicinais apresentam muitas atribuições tradicionais, incluindo o tratamento de doenças de origem infecciosa. A pesquisa científica é extremamente importante na avaliação dos usos tradicionais. Neste estudo, cinco homoisoflavonóides: 3-(4'-hidroxibenzilideno)-5,7-diidroxi-6-metoxicroman-4-ona(autumnalina), 3-(4'-hidroxibenzil)-5,7-diidroxi-6- metoxicroman-4-ona (3,9-diidro-autumnalina), 3-(3',4'-diidroxibenzil)-5,8-diidroxi-7- metoxicroman-4-ona, 3-(3',4'-diidroxibenzilideno)-5,8-diidroxi-7- metoxicroman-4-ona e 3-(3',4'-diidroxibenzilideno)-5,7-diidroxi-6- metoxicroman-4-ona foram isolados dos bulbos da planta Scilla persica HAUSSKN. Suas estruturas foram estabelecidas com base na extensa análise espectroscópica, como RMN, EM, IV e UV.Medicinal plants have many traditional claims including the treatment of ailments of infectious origin. In the evaluation of traditional claims, scientific research is extremely important. In this study, five homoisoflavonoids named 3-(4'-hydroxybenzylidene)-5,7-dihydroxy-6-methoxychroman-4-one(Autumnalin),3-(4'-hydroxybenzyl)-5,7-dihydroxy-6-methoxychroman-4-one (3,9-dihydro-autumnalin), 3-(3',4'-dihydroxybenzyl)-5,8-dihydroxy-7-methoxychroman-4-one,3-(3',4'-dihydroxybenzylidene)-5,8-dihydroxy-7-methoxychroman-4-one and 3-(3',4'-dihydroxybenzylidene)-5,7-dihydroxy-6-methoxychroman-4-one, were isolated from the bulbs of the plant Scilla persica HAUSSKN. Their structures were established on the basis of extensive spectroscopic analyses such as NMR, MS, IR and UV

Synthesis and Characterization of Polysalicylaldehyde (PSA) by Oxidative Polycondensation of Schiff base Compound [(2,4-dichlorophenylimino)methyl]-phenol

In this paper, polysalisylaldehyde (PSA) has been synthesized from the oxidative polycondensation (OP) of 2-[(2,4-dichlorophenylimino)methyl]-phenol (sal-2,4-Clan) with NaOCl in an aqueous alkaline medium between 50 and 90°C and characterized by 1H-NMR, FT-IR, UV-Vis and TGA/DTA techniques. The conversion of PSA was 61.23% in optimum conditions such as [sal-2,4-Clan]0 = 0.02, [KOH]0= 0.1 [NaOCl]0 = 0.12 mol/L at 90°C for 10 h. Additionally, the crystal structure of sal-2,4-Clan has been determined by single-crystal X-ray crystallography

Synthesis and characterization of new soluble polyamides from Acenaphtohydrazinomercaptotriazole diamine

AbstractA diamine Acenaphtohydrazinomercaptotriazole (AHTD) was synthesized in one step from acenaphthoqinone and 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole. The diamin was characterized by FTIR, 1HNMR, 13CNMR and melting point. Diamin was used to prepare novel polyamides. The low temperature solution polycondensation of diamin with tow aromatic and tow aliphatic diacid chlorides afforded diamin-containing polyamides with inherent viscosities of 0.38–0.47 dl/g in DMF at 25 °C. The polyamides were generally soluble in a wide range of solvents such as dimethylformamide(DMF), N-Methylpyrolidone(NMP), tetrachloroethane (TCE), dimethylsulfoxide(DMSO) and H2SO4. Thermal analysis showed that these polyamides were practically crustily and with Tg under 100 °C

Common method for synthesis bisphenols containing Cardo group and their polyesters with high yield

  In this paper two methods were used for the preparation of bis phenols with cardo-group and their polyesters. In comparison with other methods, a suitable method has been proposed for the preparation of these bis phenol s with higher yield and purity and also synthesis of their polymers. To achieve this goal, the 1, 1-bis (4-hydroxyphenyl) cyclohexan was used. In the first method, phenol with cyclohexanone in condensation reaction in the presence of 2 - mercapto propionic acid (the first time ) and hydrochloric/acetic acid used. First method gave higher efficiency in comparison to the second method, phenol with cyclohexanone in reflux situation in the presence of hydrochloric/acetic acid was used. Following the identification of bisphenol as a base monomer reacted with terephthaloyl dichloride as new method, solution and the phase transition polymerization. Compounds were identified by IR, NMR, CHNS and polymers were obtained by TGA test

Synthesis and characterization of novel polyester containing Schiff-base unit

Abstract A new Schiff base type of polyester containing 2,2-dimethyl-1,3-diaminopropane was prepared by solution polycondensation of 1,4-benzenedicarbonyl dichloride with Bis(4-hydroxybenzilaldehid)-2,2-dimethyl-1,3-propildiimine (H2HB2P) which is derived from a 2,2-dimethyl-1,3-diaminopropane Schiff base reacted with a 4-hydroxybenzaldehyde monomer. The monomer and the polyester were characterized by FTIR,1HNMR, and elemental analysis. The prepared polyester showed inherent viscosity of 0.29 dl/g in NMP at 25 °C, indicating their moderate molecular weight. The Polyester was completely soluble in aprotic polar solvents such asN -methylpyrolidone (NMP), dimethylformamide (DMF), Dimethyl Acetamid (DMAC), dimthylsulfoxide (DMSO). TGA determined the 10% weight loss temperature (T10) at 280 °C and residual weight at 600 °C ca. 41% under nitrogen atmosphere