The ability of octahedral complexes possessing quinone diimine ligands to inhibit transcription by stabilization of the DNA duplex structure was investigated. Rh(III) and Ru(II) complexes possessing two quinone diimine ligands in their coordination sphere were found to significantly increase the melting temperature (DeltaT(m)) of a 15-mer duplex DNA. [Rh(phi)(2)phen](3+) and [Ru(phi)(2)phen](2+) (phi = 9,10-phenanthrenequinone diimine, phen = 1,10-phenanthroline) exhibit DeltaT(m) values of +21 and +15 degrees C relative to free 15-mer duplex (T(m) = 55 degrees C) at [complex]/[DNA bases] = 0.067 (two complexes/duplex). Similarly, a shift in the melting temperature of +14 degrees C was measured for [Rh(bqdi)(2)phen](3+) (bqdi = 1,2-benzoquinone diimine), which possesses the nonintercalating bqdi ligand. In contrast, [Ru(phen)(2)phi](2+) and [Rh(phen)(2)L](3+) (L = phi, bqdi), which possess a single quinone diimine ligand, the parent [Ru(phen)(3)](2+) and [Rh(phen)(3)](3+) complexes, and ethidium bromide result in small shifts in the melting temperature of the duplex oligonucleotide. A distinct correlation between DeltaT(m) and the relative concentration of each complex required to inhibit 50% of the transcription (R(inh)(50)) was observed, independent of the presence of an intercalative ligand. The duplex stabilization by bis(quinone diimine) complexes results in inhibition of transcription in vitro at significantly lower complex concentrations than for the corresponding [Ru(phen)(2)phi](2+) and [Rh(phen)(2)L](3+) (L = phi, bqdi) complexes. Possible explanations for these observations are discussed.
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Anal Methods
January 2025
Cangzhou Jihuan Veolia Environmental Services Co., Ltd, Cangzhou, Hebei, 061108, PR China.
Nanozymes are nanomaterials with catalytic properties similar to enzymes and offer advantages over natural enzymes such as lower cost, ease of storage, and convenience for large-scale preparation. Thus, they have received increasing attention and are extensively applied in fields such as chemistry, sensing, food, environment, and medicine. Herein, a hemin-derived nanozyme (Hemin-CDs) was prepared using hemin as the precursor and used to substitute the natural horseradish peroxidase (HRP) for colorimetric detection.
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September 2024
Institute of Organometallic Chemistry of, Russian Academy of Sciences, Tropinina str, 49, 603950, Nizhny Novgorod, Russian Federation.
Synthesis and structural characterization of a family of germanium-dioxolene complexes with ditopic N-donor ligands (L-L) (L=1,2-bis(pyridin-2-ylmethylene)hydrazine L=1,6-bis-(pyridin-2-yl)-2,5-diaza-1,5-hexadiene, L=N,N-bis(pyridin-2-ylmethylene)-1,4-benzenediamine, L=N,N-bis(pyridin-2-ylmethylene)-(biphenyl)-4,4-diamine, L=2,2'-azopyridine) is reported. The reaction of germanium bis-catecholate with bridging ligands L - L, differing by the nature of the linker between pyridine sites gives rise to dinuclear digermanium complexes (36CatGe)L (36Cat=dianion of 3,6-di-tert-butylcatechol) 1-4 of DMAMD type (donor-metal-acceptor-metal-donor) with a charge transfer in the UV-Vis region. In opposite, the interaction of the 36CatGe with 2,2'-azopyridine (L) results in the two-electron transfer from the donor 36Cat ligands to the azopyridine bridge forming stable open-shell complex 5 [(36SQ)(36CatGe)](L) (36SQ=radical-anionic semiquinonate ligand).
View Article and Find Full Text PDFOrg Lett
May 2024
Department of Chemistry, National Taiwan University, Taipei, 10617, Taiwan.
The previously eight-step synthesis of bis(arylamino)pentiptycenes () from pentiptycene quinone () can now be achieved in a single step with 18-90% yields through TiCl-DABCO assisted reductive amination with anilines. Both the dual amination of and the reduction of quinone diimines are unprecedented. The π system of can be further expanded, including the formation of bis(diarylamino)pentiptycenes.
View Article and Find Full Text PDFOrg Lett
March 2024
Key Laboratory for Soft Chemistry and Functional Materials, Ministry of Education, Nanjing University of Science & Technology, Nanjing 210094, P. R. China.
A general method for the hydrogenation of quinones to hydroquinones under atmospheric pressure has been developed. In the presence of [Cp*Ir(2,2'-bpyO)(HO)] (0.5-1 mol %), a range of products were obtained in high yields.
View Article and Find Full Text PDFChemistry
April 2023
Department of Chemistry, Indian Institute of Technology Bombay Powai, Mumbai, 400076, India.
The article dealt with the ruthenium complexes of redox active azo appended modified lawsone L (HL : (E)-2-hydroxy-3-(p-tolyldiazenyl)naphthalene-1,4-dione))/L (HL :5-hydroxy-6-p-tolylazobenzo[a]phenazine) derived [Ru (acac) (L )]/[Ru (acac) (L )] 1/5, [Ru (bpy) (L )]ClO /[Ru (bpy) (L )]ClO [2]ClO /[6]ClO , ctc-[Ru (pap) (L )]ClO /ctc-[Ru (pap) (L )]ClO [3]ClO /[7]ClO and [Ru (CO)(H)(PPh ) (L )]/[Ru (CO)(Cl)(PPh ) (L )] 4/8 (acac=acetylacetonate, bpy=2,2'-bipyridine, pap=2-phenylazopyridine). The ligands L and L differed with respect to the para-quinone versus phenazine moieties linked to the azo function. Structural analysis of the complexes established unreduced state of the azo (N=N) group of coordinated L /L or pap as well as unprecedented para-quinone form of L .
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