scholarly journals Synthesis and Characterization of All Renewable Resources Based Branched Polyester: Poly(2,5-furandicarboxylic acid-co-glycerol)

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Ananda S. Amarasekara ◽  
Ashfaqur Razzaq ◽  
Paul Bonham

Condensation of all renewable resources based monomers 2,5-furandicarboxylic acid and glycerol in the presence of 2 mol% Sb2O3 catalyst at 210°C gives a branched polyester resin in 70% yield. This resin was characterized by elemental analysis, 1H, 13C NMR, FT-IR, and TGA-DTG.

2013 ◽  
Vol 17 (06n07) ◽  
pp. 555-563 ◽  
Author(s):  
İlke Gürol ◽  
Gülay Gümüş ◽  
Emel Musluoğlu ◽  
Yadigar Arslan ◽  
Vefa Ahsen

The synthesis of tetra and octa perfluoroalkyl substituted zinc and metal free phthalocyanines ( ZnPc and H 2 Pc ) are reported. The compounds 1–5 have been prepared by nucleophilic substitution of 4-nitrophthalonitrile with 1H,1H,2H,2H-perfluorooctanethiol, 1H,1H,2H,2H-perfluorodecan-1-ol, 1H,1H-perfluorodecan-1-ol, 1H,1H-perfluorotetradecan-1-ol and 1H,1H-perfluoro-3,6,9-trioxatridecan-1-ol, respectively. The compounds 6–8 have been prepared by the reaction of 1H,1H,2H,2H-perfluorodecan-1-ol, 1H,1H-perfluorodecan-1-ol and 1H,1H-perfluoro-3,6,9-trioxatridecan-1-ol with 4,5-dichlororphthalonitrile, respectively. The compound 9 with thia-bridge has been synthesized from 4,5-dichlororphthalonitrile. Zinc and metal free phthalocyanines were obtained from the corresponding phthalonitrile derivatives. All compounds were characterized by using mass, 1 H , 19 F NMR, UV-vis and FT-IR as well as elemental analysis. Tetra substituted Zn ( II ) phthalocyanines are slightly soluble only in THF (Compound 4a and 7a are insoluble) but metal free phthalocyanines are not soluble. Octa substituted Zn ( II ) and metal free phthalocyanine are soluble in polar solvents such as THF and DMSO.


2021 ◽  
Vol 14 (1) ◽  
pp. 39-47
Author(s):  
M. Fatih Polat ◽  
Derya Aktaş Anı

In this study, a new series consisting of 12 heteroaryl chalcone derivatives of 1,3,5-trimethoxybenzene were synthesised. Chalcones were synthesised in high purity and efficiency, via condensation of mono, bis and tris 2,4,6-trimethoxy acetophenones with hetero-2-carbaldehyde derivatives based on Claisen Schdmit condensation. The reactions feature a good scope for the all products, mild reaction conditions and good yields. The synthesized compounds were characterized by using FT-IR, NMR and elemental analysis spectroscopic techniques.


Author(s):  
Ankita A. Bhalu ◽  
Kalpesh Vilapara ◽  
Minaxi Maru ◽  
Manish Shah

N-(3-Bromo-4-hydroxy-5-methoxybenzylidene)-4-Bromobenzenamine was synthesized. This was further used to synthesize Co(II), Ni(II) and Co(II) based metal complexes and characterized by FT-IR, Elemental analysis, ESI Mass and UV spectroscopy.


Author(s):  
A.M. Shah ◽  
A.J. Rojivadiya

An efficient protocol for the synthesis of imidazo [1,2-a] pyrimidine was developed by using three component one-pot Biginelli synthesis. The synthesized compounds were characterized by spectroscopic techniques like FT-IR, 1H NMR, 13C NMR, and mass spectroscopy.


2017 ◽  
Vol 72 (2) ◽  
pp. 115-118 ◽  
Author(s):  
Mohammad Hakimi ◽  
Zahra Mardani ◽  
Keyvan Moeini ◽  
Fabian Mohr

AbstractIn this work, a new macrocyclic copper complex, [Cu(ACE)(SCN)2]; ACE: 1,3,6,10,12,15-hexaazatricyclo[13.3.1.16,10]eicosane, was prepared and characterized by elemental analysis, FT-IR, Raman spectroscopy and single-crystal X-ray diffraction. X-ray analysis of [Cu(ACE)(SCN)2] reveals an elongated octahedral geometry around the copper atom in a centrosymmetric CuN6 environment.


2013 ◽  
Vol 17 (06n07) ◽  
pp. 473-479 ◽  
Author(s):  
Fatma Akkuş ◽  
Nilgün Kabay ◽  
Yaşar Gök

The synthesis and characterization of novel metal-free and metallophthalocyanines, fused symmetrically in non-peripheral positions with four octaoxamacrocycle has been synthesized by cyclotetramerization of the 2,5,8,11,14,20,23,26,29,32-decaoxatricyclo [31.2.2.115,19]octatriconta-1(36),15,17,19(38),33(37),34-hexaene-34,35-dicarbonitrile (5) which was prepared by the reaction of 3,6-bis[2-(2-{2-[2-(toluene-4-sulphonyl)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-phthalonitrile (3) and 1,3-dihydroxybenzene (4). The novel compounds were characterized by using elemental analysis, 1 H , 13 C NMR, IR, UV-vis and MS spectral data.


2001 ◽  
Vol 05 (04) ◽  
pp. 367-375 ◽  
Author(s):  
S. ZEKİ YILDIZ ◽  
HALTİ KANTEKİN ◽  
YAŞAR GÖK

New metal-free 5 and metallophthalocyanines 6-11( M = Cu , Ni , Co , Pb , Zn ) fused in peripheral positions with four 24-membered tetraoxatetraaza macrocycles were prepared by cyclotetramerization of 24,25-dicyano-4,10,13,17-tetra(toluene-p-sulfonyl)-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22-didicontinehydrobenzo[y][3,9,12,18]tetraaza[1,7,16,22]tetraoxatetradicontine in the presence of the corresponding metal salt or a strong organic base. While the N-tosylated derivatives of the phthalocyanines are soluble in common organic solvents, the detosylated derivative of copper phthalocyaninate is soluble in water. The aggregation properties of the phthalocyanines were also investigated as a function of concentration, solvent and oxidative medium. The new compounds are characterized by a combination of elemental analysis and 1 H NMR, 13 C NMR, IR, UV-vis and MS spectral data.


2011 ◽  
Vol 284-286 ◽  
pp. 1782-1785
Author(s):  
Wei Chang Ke ◽  
Yi Kun Chen ◽  
Guo Xi Xiong ◽  
Xiang Hong Peng ◽  
Chao Zhu ◽  
...  

Oleoyl chloride was synthesized by oleic acid and thionyl dichloride (SOCl2), and then reacted with chitosan in dichloromethane to obtain the oleoyl chitosan. Novel water-soluble oleoyl acetyl chitosan (OACh) was synthesized using oleoyl chloride reacted with acetic anhydride in pyridine. The chemical structure of the OACh was characterized by FT-IR, 1H and 13C NMR. There existed the peaks at 1743.9 cm-1 (C=O) and 1658.1 cm-1(C=C) in FT-IR spectrum, and the peaks at 170.8, 171.6 and 172.5 ppm which were assigned to the C=O of the oleoyl and acetyl groups in 13C NMR spectrum. The results indicated that OACh had oleoyl as hydrophobic moieties and acetyl as hydrophilic moieties.


2010 ◽  
Vol 65 (5) ◽  
pp. 603-606 ◽  
Author(s):  
Yan Shen ◽  
Jun Peng ◽  
Changyun Chen ◽  
Dan Chen ◽  
Huanqiu Zhang ◽  
...  

Fluorescent nano-/microrods of the polyoxometalate (POM) K4H[Eu(α-SiW11O39)- (H2O)2] ・ 17H2O were obtained in aqueous solution by a conventional synthesis method. The nano-/microrods have been characterized by elemental analysis and FT-IR, UV/Vis, and TG-DTA data, and their morphology was examined by ESEM-FEG, showing that the average ratio of diameter to length is 1 : 20. The obtained nano-/microrods exhibit a regular profile and an intense fluorescence.


e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Valentina Siracusa ◽  
Nadia Lotti ◽  
Concetto Puglisi ◽  
Filippo Samperi ◽  
Andrea Munari ◽  
...  

AbstractThree different monomers starting from p-(4-hydroxy)benzoic acid and 3- chloro-1-propanol, 4-chloro-1-butanol and 6-chloro-1-hexanol, respectively, were synthesized and extensively characterized by means of 1H and 13C NMR, MALDITOF MS and elemental analysis. Subsequently, poly(4-oxyalkylenoxy benzoate)s polymers with different chain length were prepared in bulk starting from the mentioned above monomers, employing Ti(OBu)4 as catalyst, according to the usual two-stage polymerization procedure. The polymers were characterized in terms of chemical structure, molecular mass and thermal behaviour. Tg, Tm and the ability to crystallize were found to be affected by the number of methylene groups per repeat unit and the results were explained mainly on the basis of the increment of the chain flexibility.


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