Azine- and Imine-linked Conjugated PolyHIPEs through Schiff-Base Condensation Reaction

2021 ◽  
Author(s):  
Sebastijan Kovacic ◽  
Tomaž Kotnik ◽  
Gregor Žerjav ◽  
Albin Pintar ◽  
Ema Žagar

A new type of transition metal-free π-conjugated polyHIPEs is obtained by a Schiff-base condensation reaction coupled with a concentrated emulsion-based templating technique. The resulting highly porous azine- or imine-linked poly(arylene)...

2020 ◽  
Vol 32 (7) ◽  
pp. 1768-1772
Author(s):  
Anita Rani ◽  
Manoj Kumar ◽  
Hardeep Singh Tuli ◽  
Zahoor Abbas ◽  
Vinit Prakash

The study describes the synthesis, characterization and biological activity of a novel Schiff base ligand and its transition metal complexes. The Schiff base ligand was obtained by a condensation reaction between 4-hydroxy-3-methoxybenzaldehyde (p-vanillin) and hydrazine hydrate using ethanol as solvent. A new series of Ni(II) and Fe(III) complexes were also derived by reaction of prepared Schiff base ligand with NiCl2 and FeCl3. Both the ligand and its metal complexes were characterized by solubility, melting point and elemental analysis. These compounds were further identified by analytical techniques, FTIR, NMR and mass spectrometry. The ligand and its transition metal complexes were also subjected to in vitro biological activities i.e. antimicrobial, antiangiogenic and DNA photo cleavage. For antimicrobial activity compounds were tested against two strains of bacteria and two strains of fungi. Different concentrations of prepared compounds were treated with fertilized chicken eggs and plasmid DNA to find out antiangiogenic and DNA photocleavage activity, respectively.


2018 ◽  
Vol 9 (15) ◽  
pp. 1996-2001 ◽  
Author(s):  
Eisuke Goto ◽  
Yuto Ochiai ◽  
Mitsuru Ueda ◽  
Tomoya Higashihara

Controlled polymerization without a transition metal or halogen.


1959 ◽  
Vol 0 (0) ◽  
pp. 3753-3767 ◽  
Author(s):  
M. L. H. Green ◽  
L. Pratt ◽  
G. Wilkinson

2015 ◽  
Vol 2015 ◽  
pp. 1-14 ◽  
Author(s):  
Omoruyi G. Idemudia ◽  
Alexander P. Sadimenko ◽  
Anthony J. Afolayan ◽  
Eric C. Hosten

Two Schiff base ligands Ampp-Sn1and Bmpp-Sn2, afforded by a condensation reaction between sulfanilamide and the respective acylpyrazolone carbonyl precursors, their Mn(II), Co(II), Ni(II), and Cu(II) complexes prepared by the reaction of ligands and corresponding metal salts in aqueous solutions, were synthesized and then characterized by both analytical and spectroscopic methods, in a view to developing new improved bioactive materials with novel properties. On the basis of elemental analysis, spectroscopic and TGA results, transition metal complexes, with octahedral geometry having two molecules of the bidentate keto-imine ligand each, have been proposed. The single crystal structure of Bmpp-Sn according to X-ray crystallography showed a keto-imine tautomer type of Schiff base, having three intramolecular bonds, one short N2⋯H2⋯O3 hydrogen bond of 1.90 Å and two long C13⋯H13⋯O2 and C32⋯H32⋯O3 hydrogen bonds of 2.48 Å. A moderate to low biological activities have been exhibited by synthesized compounds when compared with standard antimicrobial agents on screening the synthesized compounds againstStaphylococcus aureus,Bacillus pumilus,Proteus vulgaris, andAeromonas hydrophilafor antibacterial activity and against free radical 1, 1-diphenyl-2-picryl-hydrazyl (DPPH) for antioxidant activity.


2011 ◽  
Vol 35 (1) ◽  
pp. 61-65 ◽  
Author(s):  
Md Mahbubul Alam

The cyclic (2+2) template condensation of pyridine-2,6-dicarboxaldehyde with 1,2-bis(2- aminoethoxy) ethane using Pb(SCN)2 as the metal source gave dinuclear lead (II) complex, Pb2L1(SCN)4 (1), where L1 is tetra-Schiff-base macrocycle. Treatment of 1 with NaBH4 in methanol gave a metal-free reduced macrocycle L2 which has been characterized by 1HNMR and ESI-MS spectroscopy.DOI: http://dx.doi.org/10.3329/jbas.v35i1.7971Journal of Bangladesh Academy of Sciences, Vol.35, No.1, 61-65, 2011


2016 ◽  
Vol 6 (15) ◽  
pp. 6152-6158 ◽  
Author(s):  
Vitthal Saptal ◽  
Digambar Balaji Shinde ◽  
Rahul Banerjee ◽  
Bhalchandra M. Bhanage

A highly porous, crystalline catechol porphyrin COF was synthesized and applied as an organocatalyst for the fixation of carbon dioxide to synthesize value-added chemicals such as cyclic carbonates and oxazolidinones under solvent and transition-metal-free conditions.


2020 ◽  
Author(s):  
Yangyang Yang ◽  
Jet Tsien ◽  
Ayala Ben David ◽  
Jonathan Hughes ◽  
Rohan Merchant ◽  
...  

Alkyl boronic acids and esters play an important role in the synthesis of C(sp<sup>3</sup>) rich medicines, agrochemicals, and other materials. This work describes a new type of transition-metal free mediated transformation to enable the construction of C(sp<sup>3</sup>)-rich, and sterically hindered alkyl boron reagents in a practical and modular manner. The broad generality and functional group tolerance of this method is extensively examined through a variety of substrates, including synthesis and late-stage functionalization of scaffolds relevant to medicinal chemistry. The strategic significance of this approach, with alkyl boronic acid as a linchpin, is demonstrated through various downstream functionalizations of the alkyl boron compounds. This two-step concurrent cross-coupling approach, resembling formal and flexible alkyl-alkyl couplings, provides a general entry to previously synthetically challenging high Fsp<sup>3</sup>-containing drug-like scaffolds.


2020 ◽  
Author(s):  
Yangyang Yang ◽  
Jet Tsien ◽  
Ayala Ben David ◽  
Jonathan Hughes ◽  
Rohan Merchant ◽  
...  

Alkyl boronic acids and esters play an important role in the synthesis of C(sp<sup>3</sup>) rich medicines, agrochemicals, and other materials. This work describes a new type of transition-metal free mediated transformation to enable the construction of C(sp<sup>3</sup>)-rich, and sterically hindered alkyl boron reagents in a practical and modular manner. The broad generality and functional group tolerance of this method is extensively examined through a variety of substrates, including synthesis and late-stage functionalization of scaffolds relevant to medicinal chemistry. The strategic significance of this approach, with alkyl boronic acid as a linchpin, is demonstrated through various downstream functionalizations of the alkyl boron compounds. This two-step concurrent cross-coupling approach, resembling formal and flexible alkyl-alkyl couplings, provides a general entry to previously synthetically challenging high Fsp<sup>3</sup>-containing drug-like scaffolds.


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