Results 11 to 20 of about 255 (109)
Pyrrolo-Fused Phenanthridines as Potential Anticancer Agents: Synthesis, Prediction, and Biological Evaluation. [PDF]
ABSTRACT We report the synthesis of four novel monoquaternary salts and four fused pyrrolo‐phenanthridine compounds, fully characterized by NMR, FT‐IR, and mass spectrometry. Guided by theoretical predictions, including molecular docking studies, we assessed their cytotoxic activity and biocompatibility.
Al-Matarneh A +6 more
europepmc +2 more sources
Fluorescent Carbazole-Derived Aza[5]Helicenes: Synthesis, Functionalization, and Characterization. [PDF]
Variously substituted indolophenanthridines, indolocarbazoles, and cinnolinocarbazoles synthesized by ortho fusion from teraryl precursors show significant Stokes shifts, especially for the protonated states of indolophenanthridines and cinnolinocarbazole.
Marten I, Dilanas MEA, Podlech J.
europepmc +2 more sources
Site-Selective Ligand Functionalization Reverses Hypsochromic Luminescence Shifts in Platinum(II) Complexes of Benzannulated NCN-Coordinating Ligands. [PDF]
Reversing the Trend: Phenanthridine (benzo[c]quinoline) donors defy conventional logic that increasing ligand benzannulation leads to bathochromic (red) shifts in the absorption and emission of their coordination complexes. Here, we provide a counterfactual that reverses this trend: substitution at the phenanthridine 6‐position (i.
Ortiz RJ +4 more
europepmc +2 more sources
In Pursuit of Low Energy Phosphorescence: Late Metal Coordination Complexes of the Planar, π-extended Bipyridyl Ligand 6,6',7,7'-Biphenanthridine. [PDF]
Abstract The coordination chemistry of the planar, doubly π‐extended bipyridine analog, 6,6′,7,7′‐biphenanthridine (p‐biphe), is presented. The phenanthridine units in p‐biphe are fused together at the 6‐ and 7‐ positions, and the resulting rigid ligand is compared with the more flexible parent “biphe” fused only at the 6‐positions.
Nemez DB +4 more
europepmc +2 more sources
Electrochemical Syntheses of Polycyclic Aromatic Hydrocarbons (PAHs)
Polycyclic aromatic hydrocarbons (PAHs) are widely applied in optoelectronics and material sciences. In the past decade, molecular electrochemistry has emerged as a novel and robust tool for PAHs synthesis. This review provides a comprehensive survey on electrochemical assembly of PAHs largely by the hydrogen evolution reaction.
Yulei Wang, Rong Zhao, Lutz Ackermann
wiley +1 more source
Currently, the global incidence of diabetes is increasing, particularly in populous developing regions. In China, over 290 million people are affected by diabetic cardio‐cerebrovascular diseases. These diseases account for more than 40% of deaths and impose a significant economic burden on both society and families.
Ying Su +7 more
wiley +1 more source
Herein we report a skeletal editing strategy for rapidly transforming readily available isoquinolines into synthetically challenging (dihydrodibenzo[c,i]phenanthridin‐6‐yl)diphenylphosphine oxides (DHBPPO) derivatives. These DHBPPO derivatives exhibit tunable emission, aggregation‐induced emission (AIE) properties, organelle‐targeted specificity, and ...
Yanling Liu +11 more
wiley +1 more source
ABSTRACT Photoremovable protecting groups (PPGs) offer a straightforward solution for the temporary inactivation of biologically active substrates and their subsequent controlled release by light irradiation. Their relatively easy design and mode of application have made them useful tools for studying dynamic biological processes in vitro and in vivo ...
Bence Kontra +3 more
wiley +1 more source
Electrochemical Hydrogenation of N‐Heterocycles and Related Substrates: A Mini‐Review
ABSTRACT Catalytic hydrogenation refers to the (often) metal‐mediated addition of dihydrogen (H2) equivalents to unsaturated compounds to form new element‐hydrogen bonds. This conceptually simple reaction is ubiquitous in the production of a vast number of essential chemicals.
Esteban Garcia‐Torres +1 more
wiley +1 more source
Ingenious introduction of an imine bond into an Ir(III)‐ferrocene complex effectively disrupts the photoinduced electron transfer process. Allowing full use of the TME to boost the efficacy of PDT, the molecule releases the Ir(III) complex and ferrocene with synergistic enhanced therapeutic effects of PDT and ferroptosis.
Yu Pei +10 more
wiley +1 more source

