Search Results - "Pagani, Giorgio A"
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Photophysics of Squaraine Dyes: Role of Charge-Transfer in Singlet Oxygen Production and Removal
Published in The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory (25-02-2010)“…The unique optical properties of squaraines render these molecules useful for applications that range from xerography to photodynamic therapy. In this regard,…”
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Bulk Heterojunction Solar Cells - Tuning of the HOMO and LUMO Energy Levels of Pyrrolic Squaraine Dyes
Published in European Journal of Organic Chemistry (01-10-2011)“…The optimization of organic photovoltaic (OPV) devices requires, amongst several factors mainly related to thin‐film blend morphology, the capability to finely…”
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π‑Conjugated Zwitterions as Paradigm of Donor–Acceptor Building Blocks in Organic-Based Materials
Published in Accounts of chemical research (18-02-2014)“…The very peculiar characteristics of zwitterions, as well as a clearand unambiguous definition, have been overlooked in past literature. However, these…”
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Panchromatic Cross‐Substituted Squaraines for Dye‐Sensitized Solar Cell Applications
Published in ChemSusChem (20-07-2009)“…Forward from square one: The incorporation of a molecularly engineered original panchromatic squaraine sensitizer in a dye‐sensitized solar cell enables the…”
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Regioselective Synthesis of 1,2- vs 1,3-Squaraines
Published in Organic letters (17-06-2011)“…Squaraines have been known for many decades as very stable and versatile vis–NIR absorbing dyes. They have found applications for example as sensitizers in…”
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Second‐Order Nonlinear Optical Activity of Dipolar Chromophores Based on Pyrrole‐Hydrazono Donor Moieties
Published in Chemistry : a European journal (15-06-2009)“…Donor1+donor2→acceptor: The second‐order NLO molecular properties of a class of dipolar chromophores that incorporate the following design elements are…”
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Effective Two-Photon Absorption Cross Section of Heteroaromatic Quadrupolar Dyes: Dependence on Measurement Technique and Laser Pulse Characteristics
Published in The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory (08-05-2008)“…The linear and nonlinear optical properties of the heteroaromatic push−pull−push two-photon absorbing dye…”
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UV absorbing zwitterionic pyridinium-tetrazolate: exceptional transparency/optical nonlinearity trade-off
Published in Chemical communications (Cambridge, England) (01-01-2011)“…We present relevant results dealing with the transparency/optical nonlinearity trade-off in high-frequency electro-optic applications. The very simple, stable…”
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Efficient Squaraine-Based Solution Processable Bulk-Heterojunction Solar Cells
Published in Journal of the American Chemical Society (31-12-2008)“…We report the fabrication of organic bulk-heterojunction solar cells based, for the first time, on squaraine/PCBM blends. The most efficient device,…”
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State-of-the-Art Neutral Tint Multichromophoric Polymers for High-Contrast See-Through Electrochromic Devices
Published in Advanced functional materials (02-08-2016)“…Two new multichromophoric electrochromic polymers featuring a conjugated EDOT/ProDOT copolymer backbone (PXDOT) and a reversible Weitz‐type redox active small…”
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A High Molecular Weight Donor for Electron Injection Interlayers on Metal Electrodes
Published in Chemphyschem (07-12-2009)“…The molecular donor 9,9′‐ethane‐1,2‐diylidene‐bis(N‐methyl‐9,10‐dihydroacridine) (NMA) has been synthesized, and its electronic properties were characterized…”
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Gray to Colorless Switching, Crosslinked Electrochromic Polymers with Outstanding Stability and Transmissivity From Naphthalenediimmide-Functionalized EDOT
Published in Advanced materials (Weinheim) (17-04-2012)“…The design, synthesis, polymerization and full electrochemical and spectroelectrochemical characterization of a new naphtalendiimide‐functionalized PEDOT…”
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Assessment of Water-Soluble π-Extended Squaraines as One- and Two-Photon Singlet Oxygen Photosensitizers: Design, Synthesis, and Characterization
Published in Journal of the American Chemical Society (13-02-2008)“…Singlet oxygen sensitization by organic molecules is a topic of major interest in the development of both efficient photodynamic therapy (PDT) and aerobic…”
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Photooxidation and Phototoxicity of π-Extended Squaraines
Published in Journal of medicinal chemistry (11-03-2010)“…This paper describes the synthesis of π-extended squaraines and their photooxidation properties and gives an in-depth characterization of these molecules as…”
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Extended Squaraine Dyes with Large Two-Photon Absorption Cross-Sections
Published in Journal of the American Chemical Society (15-11-2006)“…Extended bis(donor)-substituted squaraine chromophores exhibit very high two-photon cross-sections (as high as 33 000 GM) in the near-IR; these can be…”
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Marked Alkyl- vs Alkenyl-Substitutent Effects on Squaraine Dye Solid-State Structure, Carrier Mobility, and Bulk-Heterojunction Solar Cell Efficiency
Published in Journal of the American Chemical Society (31-03-2010)“…We report two new squaraine dyes substituted at the pyrrolic rings with n-hexyl (squaraine 1) or n-hexenyl (squaraine 2) chains. Although internal molecular…”
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Enhancement of Two-Photon Absorption Cross-Section and Singlet-Oxygen Generation in Porphyrins upon β-Functionalization with Donor−Acceptor Substituents
Published in Organic letters (22-06-2006)“…The microwave-enhanced synthesis, comparative singlet oxygen sensitization efficiency, and nonlinear optical characterization of a new β-functionalized…”
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Novel Heterocycle-Based Two-Photon Absorbing Dyes
Published in Organic letters (02-05-2002)“…The synthesis and nonlinear optical characterization of two novel heteroaromatic-based chromophores is described. The new dyes present an A−π−D−π−A general…”
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Exomethylene-3,4-ethylenedioxythiophene (emEDOT): A New Versatile Building Block for Functionalized Electropolymerized Poly(3,4-ethylenedioxythiophenes) (PEDOTs)
Published in Organic letters (19-07-2013)“…A new versatile thiophene derivative exomethylene-3,4-ethylenedioxythiophene (emEDOT) is introduced. The molecule can be straightforwardly prepared in two…”
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