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Phenylboronic Acid Modified Anodes Promote Faster Biofilm Adhesion and Increase Microbial Fuel Cell Performances.
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- Electroanalysis, 2013, v. 25, n. 3, p. 601, doi. 10.1002/elan.201200351
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- Article
[n]‐Cyclo‐9,9‐dibutyl‐2,7‐fluorene (n=4, 5): Nanoring Size Influence in Carbon‐Bridged Cyclo‐para‐phenylenes.
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- Angewandte Chemie, 2020, v. 132, n. 27, p. 11159, doi. 10.1002/ange.202002517
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- Article
C1‐Linked Spirobifluorene Dimers: Pure Hydrocarbon Hosts for High‐Performance Blue Phosphorescent OLEDs.
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- Angewandte Chemie, 2019, v. 131, n. 12, p. 3888, doi. 10.1002/ange.201813604
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- Article
ortho-, meta-, and para-Dihydroindenofluorene Derivatives as Host Materials for Phosphorescent OLEDs.
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- Angewandte Chemie, 2015, v. 127, n. 4, p. 1192, doi. 10.1002/ange.201409479
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- Article
Blue Emitting 3 π-2 Spiro Terfluorene-Indenofluorene Isomers: A Structure-Properties Relationship Study.
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- Chemistry - A European Journal, 2011, v. 17, n. 50, p. 14031, doi. 10.1002/chem.201102212
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- Article
Incorporation of Spiroxanthene Units in Blue-Emitting Oligophenylene Frameworks: A New Molecular Design for OLED Applications.
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- Chemistry - A European Journal, 2011, v. 17, n. 45, p. 12631, doi. 10.1002/chem.201100790
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- Article
Violet-to-Blue Tunable Emission of Aryl-Substituted Dispirofluorene-Indenofluorene Isomers by Conformationally-Controllable Intramolecular Excimer Formation.
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- Chemistry - A European Journal, 2011, v. 17, n. 37, p. 10272, doi. 10.1002/chem.201100971
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- Article
(2,1- a)-Indenofluorene Derivatives: Syntheses, X-ray Structures, Optical and Electrochemical Properties.
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- Chemistry - A European Journal, 2010, v. 16, n. 46, p. 13646, doi. 10.1002/chem.201001830
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- Article
Encumbered DiSpiro[Fluorene-IndenoFluorene]: Mechanistic Insights.
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- Chemistry - A European Journal, 2009, v. 15, n. 48, p. 13304, doi. 10.1002/chem.200902006
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- Article
[4]Cyclofluorene: Unexpected Influence of Alkyl Chain Length.
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- ChemPlusChem, 2018, v. 83, n. 9, p. 874, doi. 10.1002/cplu.201800369
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- Article
Modulation of the Physicochemical Properties of Donor-Spiro- Acceptor Derivatives through Donor Unit Planarisation: Phenylacridine versus Indoloacridine--New Hosts for Green and Blue Phosphorescent Organic Light-Emitting Diodes (PhOLEDs).
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- Chemistry - An Asian Journal, 2016, v. 6, p. 10136, doi. 10.1002/chem.201600652
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- Article
A glance at violet LED sensitive photoinitiators based on the spiroxanthene scaffold.
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- Journal of Applied Polymer Science, 2016, v. 133, n. 12, p. 1, doi. 10.1002/app.43213
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- Article
ortho-, meta-, and para-Dihydroindenofluorene Derivatives as Host Materials for Phosphorescent OLEDs.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 4, p. 1176, doi. 10.1002/anie.201409479
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- Article
Dependence of the Properties of Dihydroindenofluorene Derivatives on Positional Isomerism: Influence of the Ring Bridging.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 52, p. 14147, doi. 10.1002/anie.201306668
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- Article
Stability of Tin Etiopurpurin.
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- Photochemistry & Photobiology, 2005, v. 81, n. 1, p. 149, doi. 10.1111/j.1751-1097.2005.tb01534.x
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- Article
Front Cover: Electronic and Charge Transport Properties in Bridged versus Unbridged Nanohoops: Role of the Nanohoop Size (Chem. Eur. J. 41/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 41, p. 1, doi. 10.1002/chem.202301809
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- Article
Electronic and Charge Transport Properties in Bridged versus Unbridged Nanohoops: Role of the Nanohoop Size.
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- Chemistry - A European Journal, 2023, v. 29, n. 41, p. 1, doi. 10.1002/chem.202300934
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- Article
[4]‐Cyclo‐2,7‐Carbazole as Host Material in High‐Efficiency Phosphorescent OLEDs: A New Perspective for Nanohoops in Organic Electronics.
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- Advanced Optical Materials, 2023, v. 11, n. 3, p. 1, doi. 10.1002/adom.202202191
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- Article
Spirophenylacridine‐2,7‐(diphenylphosphineoxide)‐fluorene: A Bipolar Host for High‐Efficiency Single‐Layer Blue Phosphorescent Organic Light‐Emitting Diodes.
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- Advanced Optical Materials, 2020, v. 8, n. 2, p. N.PAG, doi. 10.1002/adom.201901225
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- Article
Pure Hydrocarbon Materials as Highly Efficient Host for White Phosphorescent Organic Light‐Emitting Diodes: A New Molecular Design Approach.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 35, p. 1, doi. 10.1002/anie.202207204
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- Article
[n]‐Cyclo‐9,9‐dibutyl‐2,7‐fluorene (n=4, 5): Nanoring Size Influence in Carbon‐Bridged Cyclo‐para‐phenylenes.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 27, p. 11066, doi. 10.1002/anie.202002517
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- Publication type:
- Article
C1‐Linked Spirobifluorene Dimers: Pure Hydrocarbon Hosts for High‐Performance Blue Phosphorescent OLEDs.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 12, p. 3848, doi. 10.1002/anie.201813604
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- Publication type:
- Article
Dependence of the Properties of Dihydroindenofluorene Derivatives on Positional Isomerism: Influence of the Ring Bridging.
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- Angewandte Chemie, 2013, v. 125, n. 52, p. 14397, doi. 10.1002/ange.201306668
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- Publication type:
- Article
Positional Isomers of Phenylacridine/Spirobifluorene as Deep‐Blue Fluorescent Emitters for Organic Light‐Emitting Diodes.
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- Advanced Materials Technologies, 2023, v. 8, n. 19, p. 1, doi. 10.1002/admt.202300763
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- Article
Quinolinoacridine as High Efficiency Building Unit in Single‐Layer Phosphorescent Organic Light‐Emitting Diodes.
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- Advanced Electronic Materials, 2024, v. 10, n. 1, p. 1, doi. 10.1002/aelm.202300582
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- Article
New 3π-2Spiro Ladder-Type Phenylene Materials: Synthesis, Physicochemical Properties and Applications in OLEDs.
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- Chemistry - A European Journal, 2008, v. 14, n. 36, p. 11328, doi. 10.1002/chem.200801428
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- Article
Dispirofluorene-Indenofluorene Derivatives as New Building Blocks for Blue Organic Electroluminescent Devices and Electroactive Polymers.
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- Chemistry - A European Journal, 2007, v. 13, n. 36, p. 10055, doi. 10.1002/chem.200701036
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- Article
Cyclization of Terphenyl‐Bisfluorenols: A Mechanistic Study of the Regioselectvity.
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- Chemistry - A European Journal, 2019, v. 25, n. 45, p. 10689, doi. 10.1002/chem.201901457
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- Article
[4]Cyclo‐N‐ethyl‐2,7‐carbazole: Synthesis, Structural, Electronic and Charge Transport Properties.
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- Chemistry - A European Journal, 2019, v. 25, n. 32, p. 7740, doi. 10.1002/chem.201901066
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- Article
Modulating the Physical and Electronic Properties over Positional Isomerism: The Dispirofluorene-Dihydroindacenodithiophene (DSF-IDT) Family.
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- Chemistry - A European Journal, 2017, v. 23, n. 68, p. 17290, doi. 10.1002/chem.201703320
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Inside Back Cover: Spirobifluorene Regioisomerism: A Structure-Property Relationship Study (Chem. Eur. J. 32/2017).
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- Chemistry - A European Journal, 2017, v. 23, n. 32, p. 7830, doi. 10.1002/chem.201701470
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- Article
Spirobifluorene Regioisomerism: A Structure-Property Relationship Study.
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- Chemistry - A European Journal, 2017, v. 23, n. 32, p. 7719, doi. 10.1002/chem.201700570
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- Article
9 H-Quinolino[3,2,1- k]phenothiazine: A New Electron-Rich Fragment for Organic Electronics.
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- Chemistry - A European Journal, 2016, v. 22, n. 50, p. 17930, doi. 10.1002/chem.201603659
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- Article
Inside Back Cover: 9 H-Quinolino[3,2,1- k]phenothiazine: A New Electron-Rich Fragment for Organic Electronics (Chem. Eur. J. 50/2016).
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- Chemistry - A European Journal, 2016, v. 22, n. 50, p. 18267, doi. 10.1002/chem.201604608
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- Article
Modulation of the Physicochemical Properties of Donor-Spiro-Acceptor Derivatives through Donor Unit Planarisation: Phenylacridine versus Indoloacridine--New Hosts for Green and Blue Phosphorescent Organic Light-Emitting Diodes (PhOLEDs).
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- Chemistry - A European Journal, 2016, v. 22, n. 29, p. 10136, doi. 10.1002/chem.201600652
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- Publication type:
- Article
Donor/Acceptor Dihydroindeno[1,2- a]fluorene and Dihydroindeno[2,1- b]fluorene: Towards New Families of Organic Semiconductors.
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- Chemistry - A European Journal, 2015, v. 21, n. 26, p. 9426, doi. 10.1002/chem.201500336
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- Article
Spirobifluorene Dimers: Understanding How The Molecular Assemblies Drive The Electronic Properties.
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- Advanced Functional Materials, 2021, v. 31, n. 43, p. 1, doi. 10.1002/adfm.202104980
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- Article
Designing Host Materials for the Emissive Layer of Single‐Layer Phosphorescent Organic Light‐Emitting Diodes: Toward Simplified Organic Devices.
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- Advanced Functional Materials, 2021, v. 31, n. 24, p. 1, doi. 10.1002/adfm.202010547
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- Article
Blue Single‐Layer Organic Light‐Emitting Diodes Using Fluorescent Materials: A Molecular Design View Point.
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- Advanced Functional Materials, 2020, v. 30, n. 17, p. 1, doi. 10.1002/adfm.201910040
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- Article
Spirobifluorene Trimers: High Triplet Pure Hydrocarbon Hosts for Highly Efficient Blue Phosphorescent Organic Light‐Emitting Diodes.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 31, p. 1, doi. 10.1002/anie.202403066
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- Article
π‐Conjugated Nanohoops: A New Generation of Curved Materials for Organic Electronics.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 30, p. 1, doi. 10.1002/anie.202402608
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- Article
Spirobifluorene Trimers: High Triplet Pure Hydrocarbon Hosts for Highly Efficient Blue Phosphorescent Organic Light‐Emitting Diodes.
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- Angewandte Chemie, 2024, v. 136, n. 31, p. 1, doi. 10.1002/ange.202403066
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- Article
π‐Conjugated Nanohoops: A New Generation of Curved Materials for Organic Electronics.
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- Angewandte Chemie, 2024, v. 136, n. 30, p. 1, doi. 10.1002/ange.202402608
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- Publication type:
- Article
Pure Hydrocarbon Materials as Highly Efficient Host for White Phosphorescent Organic Light‐Emitting Diodes: A New Molecular Design Approach.
- Published in:
- Angewandte Chemie, 2022, v. 134, n. 35, p. 1, doi. 10.1002/ange.202207204
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- Article
Direct Electron Transfer of Hemoglobin and Myoglobin at the Bare Glassy Carbon Electrode in an Aqueous BMI.BF.
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- ChemPhysChem, 2011, v. 12, n. 2, p. 411, doi. 10.1002/cphc.201000779
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- Article
Highly Efficient Thermally Activated Delayed Fluorescence via an Unconjugated Donor–Acceptor System Realizing EQE of Over 30%.
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- Advanced Materials, 2020, v. 32, n. 48, p. 1, doi. 10.1002/adma.202003885
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- Article
Grafting Electron‐Accepting Fragments on [4]cyclo‐2,7‐carbazole Scaffold: Tuning the Structural and Electronic Properties of Nanohoops.
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- Advanced Science, 2024, v. 11, n. 13, p. 1, doi. 10.1002/advs.202309115
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- Article