The synthesis, photophysics and biological investigation of fluorescent 4-amino-1,8-naphthalimide Tröger's bases (TB-1-TB-3) and a new Tröger's base p-cymene-Ru(ii)-curcumin organometallic conjugate (TB-Ru-Cur) are described; these compounds showed fast cellular uptake and displayed good luminescence and cytotoxicity against cervical cancer cells. © 2018 The Royal Society of Chemistry.

Shanmugaraju Sankarasekaran

Department of Chemistry

B. La Cour Poulsen

T. Arisa

D. Umadevi

H.L. Dalton

C.S. Hawes

S. Estalayo-Adrián

A.J. Savyasachi

G.W. Watson

D.C. Williams

Fulltext

Indian Institute of Technology Palakkad&nbsp;(IIT Palakkad or IIT PKD) is a public autonomous&nbsp;engineering&nbsp;and&nbsp;research&nbsp;institute located in&nbsp;Palakkad,&nbsp;Kerala. It was&nbsp;one of the five new&nbsp;IITs&nbsp;proposed in the&nbsp;2014 Union budget of India. The campus was inaugurated on 3 August 2015. The institute has 94 faculty, 978 students, and 63 non-teaching staffs.

IT Palakkad currently offers four-year Bachelor of Technology (B.Tech) and two years MS programmes in 8 different engineering disciplines including&nbsp;Computer Science, Electrical, Mechanical, Civil among others.

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IIT Palakkad

Chemical Communications

The solvothermal synthesis and structural characterization of two new supramolecular coordination polymers featuring a unique V-shaped ligand bis-[N-(3-pyridyl)methyl)]-9,18-methano-1,8-naphthalimide-[b,f][1,5]diazocine (TBNap), are reported. The ligand TBNap was synthesized as a racemic mixture and the molecular structure was analyzed crystallographically. TBNap showed a positive solvatochromism effect which was further supported by DFT calculations illustrating the D-π-A type fluorophore effects within the ligand structures. TBNap was further employed as a potential fluorescence probe for the discriminative sensing of structurally assorted antibiotics. A strong fluorescence quenching and preferential binding affinity were realized for nitro-containing antibiotics, i.e., Furazolidone, Nitrofurantoin and Nitrofurazone. The solvothermal reaction of TBNap with Cd(OAc)2‧2H2O afforded a one-dimensional coordination polymer (TB-CP-1, poly-[Cd(TBNap)(OAc)2]). Similarly, reaction between TBNap and CdCl2.4H2O in DMF-C2H5OH rendered a 4,4’-2D coordination sheet (TB-CP-2, poly-[CdCl2(TBNap)]·DMF). The extended polymeric structures are further propagated into 3D supramolecular network through multiple face-to-face π-π interaction. © 2021 Informa UK Limited, trading as Taylor & Francis Group.

Supramolecular Chemistry

Synthesis, structural characterization, antibiotics sensing and coordination chemistry of a fluorescent 4-amino-1,8-naphthalimide Tröger’s base supramolecular scaffold

We report here a novel one-pot synthetic strategy for the synthesis of a family of N-alkyl-1,8-naphthalimide based Tröger's bases via a nucleophilic substitution reaction of a common 'precursor' (or a 'synthon') N-aryl-1,8-naphthalimide Tröger's base heated at 80 °C in neat aliphatic primary amine, in overall yield of 65-96%. This methodology provides an efficient and one-step facile route to design 1,8-naphthalimide derived Tröger's base structures in analytically pure form without the use of column chromatography purification, that can be used in medicinal chemistry and as supramolecular scaffolds. We also report the formation of the corresponding anhydride, and the crystallographic analysis of two of the resulting products, that of the N-phenyl-4-amino-1,8-naphthalimide and the anhydride derived Tröger's bases. © 2017 The Royal Society of Chemistry.

Organic and Biomolecular Chemistry

One-pot facile synthesis of 4-amino-1,8-naphthalimide derived Tröger's bases: Via a nucleophilic displacement approach

A V-Shaped 4-amino-1,8-napthalimide derived tetracarboxylic acid linker (L; bis-[N-(1,3-benzenedicarboxylic acid)]-9,18-methano-1,8-naphthalimide-[b,f][1,5]diazocine) comprising the Tröger's base (TB) structural motif was rationally designed and synthesised to access a nitrogen-rich fluorescent supramolecular coordination polymer. By adopting the straight forward precipitation method, a new luminescent nanoscale Zn(ii) coordination polymer (TB-Zn-CP) was synthesized in quantitative yield using Zn(OAc)2·2H2O and tetraacid linker L (1 : 0.5) in DMF at room temperature. The phase-purity of as-synthesised TB-Zn-CP was confirmed by X-ray powder diffraction analysis, infra-red spectroscopy, and elemental analysis. Thermogravimetric analysis suggests that TB-Zn-CP is thermally stable up to 330 °C and the morphological features of TB-Zn-CP was analysed by SEM and AFM techniques. The N2 adsorption isotherm of thermally activated TB-Zn-CP at 77 K revealed a type-II reversible adsorption isotherm and the calculated Brunauer-Emmett-Teller (BET) surface area was found to be 72 m2 g−1. Furthermore, TB-Zn-CP displayed an excellent CO2 uptake capacity of 76 mg g−1 at 273 K and good adsorption selectivity for CO2 over N2 and H2. The aqueous suspension of as-synthesized TB-Zn-CP showed strong green fluorescence (λmax = 520 nm) characteristics due to the internal-charge transfer (ICT) transition and was used as a fluorescent sensor for the discriminative sensing of nitroaromatic explosives. The aqueous suspension of TB-Zn-CP showed the largest quenching responses with high selectivity for phenolic-nitroaromatics (4-NP, 2,4-DNP and PA) even in the concurrent presence of other potentially competing nitroaromatic analytes. The fluorescence titration studies also provide evidence that TB-Zn-CP detects picric acid as low as the parts per billion (26.3 ppb) range. Furthermore, the observed fluorescence quenching responses of TB-Zn-CP towards picric acid were highly reversible. The highly selective fluorescence quenching responses including the reversible detection efficiency make the nanoscale coordination polymer TB-Zn-CP a potential material for the discriminative fluorescent sensing of nitroaromatic explosives. © The Royal Society of Chemistry.

Chemical Science

A supramolecular Tröger's base derived coordination zinc polymer for fluorescent sensing of phenolic-nitroaromatic explosives in water

Chemical Society Reviews

The development of ruthenium(ii) polypyridyl complexes and conjugates forin vitrocellular andin vivoapplications

The development of anticancer ruthenium(ii) complexes: from single molecule compounds to nanomaterials

Inorganic Chemistry

New Class of Half-Sandwich Ruthenium(II) Arene Complexes Bearing the Water-Soluble CAP Ligand as an in Vitro Anticancer Agent

Synthesis, structural characterisation and antiproliferative activity of a new fluorescent 4-amino-1,8-naphthalimide Tröger's base-Ru(ii)-curcumin organometallic conjugate

Journal	Data powered by TypesetChemical Communications
Publisher	Data powered by TypesetRoyal Society of Chemistry
ISSN	13597345
Open Access	No