Search Results - "Zagranyarski, Yulian"
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On-Surface Synthesis of Rylene-Type Graphene Nanoribbons
Published in Journal of the American Chemical Society (01-04-2015)“…The narrowest armchair graphene nanoribbon (AGNR) with five carbons across the width of the GNR (5-AGNR) was synthesized on Au(111) surfaces via sequential…”
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Structure–property correlation to assist the design of organic blue emitters with thermally activated delayed fluorescence
Published in Theoretical chemistry accounts (01-11-2024)“…Organic light-emitting diodes are constantly developed technologically. An advantageous strategy for efficient work of the devices is the design of emitters…”
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3
Dioxepine-Peri-Annulated PMIs-Synthesis and Spectral and Sensing Properties
Published in Sensors (Basel, Switzerland) (07-03-2023)“…New perylene monoimide (PMI) derivatives bearing a seven-membered heterocycle and 1,8-diaminosarcophagine (DiAmSar) or N,N-dimethylaminoethyl chelator…”
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Naphthalimide-Based Amphiphiles: Synthesis and DFT Studies of the Aggregation and Interaction of a Simplified Model System with Water Molecules
Published in Molecules (Basel, Switzerland) (04-09-2024)“…Systems containing amphiphilic/pathic molecules have the tremendous capacity to self-assemble under appropriate conditions to form morphologies with…”
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Ultra‐Narrow Low‐Bandgap Graphene Nanoribbons from Bromoperylenes—Synthesis and Terahertz‐Spectroscopy
Published in Chemistry : a European journal (06-04-2017)“…Soluble ultra‐narrow armchair graphene nanoribbons (AGNRs) with length of ≈20 nm and completely fused cores exceeding 5 nm in length, pronounced near‐infrared…”
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Estrone derived 2-naphthol analogue in the diastereoselective one-pot Betti-condensation
Published in Molecular diversity (01-11-2020)“…The utility of deoxy-isoequilenine synthesized from estrone as valuable 2-naphthol analogue is demonstrated in the three components Betti-condensation. A…”
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Hydrogen‐Bonded Donor–Acceptor Arrays at the Solution–Graphite Interface
Published in Chemistry : a European journal (14-08-2018)“…Controlling the nanoscale morphology of organic thin films represents a critical challenge in the fabrication of organic (opto)electronic devices. The…”
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N-Annulation of the BTI Rylene Imide Organic Building Block: Impact on the Optoelectronic Properties of π-Extended Molecular Structures
Published in Colorants (30-12-2022)“…Benzothioxanthene imide (BTI) has recently emerged as an interesting and promising block for organic electronics. In this contribution, we report on the impact…”
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Microwave-Assisted, Copper-Catalyzed Domino O–H/C–H Arylation Reaction toward the Synthesis of Oxygen-Doped Polyaromatic Molecules
Published in Journal of organic chemistry (18-08-2023)“…Benzoxanthenes and their analogues are a very important class of compounds mainly due to their wide range of biological and technological applications. The…”
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One-pot synthesis of fused-rings heterocyclic systems based on symmetrically benzofuran annulated 1,8-naphthalimides
Published in Dyes and pigments (01-12-2023)“…A useful and straightforward synthetic approach to afford heteroarenes by symmetrical annulation of two benzofuran units to 1,8-naphthalene anhydrides, through…”
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Toward a Tunable Synthetic [FeFe]-Hydrogenase H‑Cluster Mimic Mediated by Perylene Monoimide Model Complexes: Insight into Molecular Structures and Electrochemical Characteristics
Published in Organometallics (08-10-2018)“…The nature of the bridging dithiolate has an important role on tuning the physical and electrochemical properties of the synthetic H-cluster mimics of…”
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Dioxin-annulated 1,8-naphthalimides – Synthesis, spectral and electrochemical properties, and application in OLED
Published in Dyes and pigments (01-01-2021)“…A synthetic approach for preparation of a new class of 1,8-naphthalimide derivatives with fused benzo and naphtho-dioxin systems is reported. The proposed…”
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Naphthalene Monoimides with Peri -Annulated Disulfide Bridge-Synthesis and Electrochemical Redox Activity
Published in Materials (01-12-2023)“…Nowadays, organosulfur compounds provide new options in the development of full organic ion batteries. However, many drawbacks (such as kinetics limitations…”
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Carbonyl-Functionalized Cyclazines as Colorants and Air-Stable n‑Type Semiconductors
Published in Organic letters (02-03-2018)“…A series of π-extended cycl[3,3,2]azines (3) bearing additional carbonyl groups were synthesized via aldol condensations. Two strong electron acceptor…”
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Perylene pigments as alternatives to phthalocyanine and indanthrone blue
Published in Dyes and pigments (01-12-2021)“…A series of new chromophores were synthesized which comprise carboximide and ureido auxochromic moieties attached to a perylene core. The blue perylene pigment…”
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Naphthalene Monoimides with IPeri/I-Annulated Disulfide Bridge—Synthesis and Electrochemical Redox Activity
Published in Materials (01-12-2023)“…Nowadays, organosulfur compounds provide new options in the development of full organic ion batteries. However, many drawbacks (such as kinetics limitations…”
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Self-Assembly of an Amphiphilic π-Conjugated Dyad into Fibers: Ultrafast and Ultrasensitive Humidity Sensor
Published in Advanced materials (Weinheim) (27-05-2015)“…The self‐assembly of an amphiphilic monomolecular electron acceptor–donor dyad into electroactive π–π stacked fibrillar structures can be triggered by…”
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Water-Soluble NIR-Absorbing Rylene Chromophores for Selective Staining of Cellular Organelles
Published in Journal of the American Chemical Society (09-03-2016)“…Biocompatible organic dyes emitting in the near-infrared are highly desirable in fluorescence imaging techniques. Herein we report a synthetic approach for…”
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Benchmarking of Density Functionals for the Description of Optical Properties of Newly Synthesized π‐Conjugated TADF Blue Emitters
Published in Chemistry : a European journal (16-03-2022)“…Computational modeling of the optical characteristics of organic molecules with potential for thermally activated delayed fluorescence (TADF) may assist…”
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TADF Blue Emitters with Balanced π-Conjugation─Design, Synthesis, Spectral Characterization, and a Model OLED with 8-(5-(tert-Butyl)-1,3,4-oxadiazol-2-yl)-N,N-bis(4-(tert-butyl)phenyl)dibenzob,dfuran-2-amine
Published in The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory (04-07-2024)“…Blue organic light-emitting diodes (OLED) suffer from relatively short lifetimes and a comparatively low lighting efficiency. One of the approaches to…”
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