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Fusion and planarization of bisBODIPY: a new family of photostable near infrared dyes.Porphyrin-based sensor nanoarchitectonics in diverse physical detection modes.Biological Evaluation of Dipyrromethanes in Cancer Cell Lines: Antiproliferative and Pro-apoptotic Properties.Ligand size dependence of U-N and U-O bond character in a series of uranyl hexaphyrin complexes: quantum chemical simulation and density based analysis.Dynamic neighbouring participation of nitrogen lone pairs on the chromogenic behaviour of trans-bis(salicylaldiminato)Pt(ii) coordination platforms.Unprecedented Double aza-Michael Addition within a Sapphyrin Core.Thieno-pyrrole-fused BODIPY intermediate as a platform to multifunctional NIR agents.Core-modified analogues of expanded porphyrins containing rigid β,β'-linked o-phenylene bridges.Structural, Photophysical, and Magnetic Circular Dichroism Studies of Three Rigidified meso-Pentafluorophenyl-Substituted Hexaphyrin Analogues.ESI-MS/MS of expanded porphyrins: a look into their structure and aromaticity.Solvent-Sensitive Emitting Urea-Bridged bis-BODIPYs: Ready Access by a One-Pot Tandem Staudinger/Aza-Wittig Ureation.meso-Aryl [20]π Homoporphyrin: The Simplest Expanded Porphyrin with the Smallest Möbius Topology.Effects of cyano, ethynyl and ethylenedioxy groups on the photophysical properties of carbazole-based porphyrins.Switching between porphyrin, porphodimethene and porphyrinogen using cyanide and fluoride ions mimicking volatile molecular memory and the 'NOR' logic gate.Our Expedition in Linear Neutral Platinum-Acetylide Complexes: The Preparation of Micro/nanostructure Materials, Complicated Topologies, and Dye-Sensitized Solar Cells.Thiophene-fused dithiaoctaphyrins: π-system switching between cross-conjugated and macrocyclic π-networks.Gadolinium(III) Porpholactones as Efficient and Robust Singlet Oxygen Photosensitizers.Ruthenocene-Type Complexes of N-Fused Porphyrins.Covalent Porphyrin Hybrids Linked with Dipyrrin, Bidipyrrin or Thiacorrole.Isoxazolidine-fused meso-tetraarylchlorins as key tools for the synthesis of mono- and bis-annulated chlorins.Quaternized Pyridyloxy Phthalocyanines Render Aqueous Electron-Donor Carbon Nanotubes as Unprecedented Supramolecular Materials for Energy ConversionSelf-assembly and characterization of small and monodisperse dye nanospheres in a protein cageOptical signatures of Boron adducts of Oxasmaragdyrin: insights from theory
P2860
Q31001525-07022EA7-F6D3-4376-B472-DB6D5B980C8BQ38190432-EF9309D1-120E-409E-97F9-D2CA14F3EC99Q38708843-28565A87-26B8-46D3-A4BD-5C316AF1999FQ38933930-E7A41C1A-EA44-47D3-B68D-28FDF222AAD1Q39149798-98694B6B-D574-4D60-B1CE-5DA68BF7A81DQ39481866-139F397C-6C7E-4AA6-B376-0AE4A7EE46A0Q44258248-B8ED1FFD-03D2-43E1-BEE9-18B8CE4C472EQ45059414-48E040CF-7C09-4D6A-AE6C-B8EF72BCE318Q46401874-DFFBC5FD-B4BA-4B79-9C05-5E6E02516394Q46546291-DE9318A8-8F5C-41CD-8376-1916210EE5D6Q48156913-3CBEEE4D-D071-4444-A067-3081461EB30EQ50088313-E905115A-C0DC-4612-A082-D1DD23746DC3Q50209149-D0F4BE3C-F370-49E5-96D2-BCC290612CBCQ50226928-D4C5C190-EDBD-4AEC-83DC-11C3B0B91C76Q50229404-8472EE81-E736-4FDE-80A4-E371747B0EE8Q50793261-8CE3AB7A-40A4-49CF-9F32-4B263D88C930Q51308864-57DDF508-5C8A-469D-B4F8-E7E96865FEAEQ51349317-D9EF415E-03E9-449F-8A85-B0C0F571CE78Q52537429-395908E5-3E38-43DD-8901-9CE81EA75FE4Q52938075-598267D6-8BE6-4922-BBE1-9AC96B3D3AF2Q57615862-A224AE02-106B-4950-9201-EFECE41D37A1Q57615925-751A461F-7101-4B75-B915-0E8EDB5BA073Q57770773-5C9B824E-1955-48BC-AD7C-8C7959878570
P2860
description
article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
π-Extended isomeric and expanded porphyrins.
@en
type
label
π-Extended isomeric and expanded porphyrins.
@en
prefLabel
π-Extended isomeric and expanded porphyrins.
@en
P2093
P2860
P356
P1476
π-Extended isomeric and expanded porphyrins.
@en
P2093
Chang-Hee Lee
Jonathan L Sessler
Vladimir V Roznyatovskiy
P2860
P304
P356
10.1039/C2CS35418G
P577
2012-12-11T00:00:00Z