Relevant bibliographies by topics / Subphthalocyanine

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Subphthalocyanine'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Subphthalocyanine"

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Rudolf, Marc, Olga Trukhina, Josefina Perles, et al. "Taming C60fullerene: tuning intramolecular photoinduced electron transfer process with subphthalocyanines." Chemical Science 6, no. 7 (2015): 4141–47. http://dx.doi.org/10.1039/c5sc00223k.

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Two subphthalocyanine–C<sub>60</sub>fullerene electron donor–acceptor conjugates have been prepared from electron deficient subphthalocyanines and C<sub>60</sub>, with evidence of an ultrafast oxidative electron transfer from C<sub>60</sub>to the subphthalocyanines.
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Sánchez-Molina, Irene, Guillermo Lucena-Alcalde, Christian G. Claessens, and Tomás Torres. "Effect of a chiral ligand in the self-assembly of subphthalocyanine-based metallosupramolecular capsules." Canadian Journal of Chemistry 92, no. 8 (2014): 685–87. http://dx.doi.org/10.1139/cjc-2014-0053.

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Subphthalocyanine-based metallosupramolecular capsules have been self-assembled employing a chiral phosphine (S-BINAP). This ligand seems to provide an arrangement of the coordination positions of platinum that inverts the known process of chiral self-discrimination of subphthalocyanines, which is typically produced between the enantiomers of the macrocycle when a nonchiral ligand is used for the self-assembly. In this article, we describe preliminary studies on the effect of S-BINAP on the self-assembly subphthalocyanine capsules.
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Göktuğ, Özge, Cem Göl, and Mahmut Durmuş. "Synthesis of novel dimeric subphthalocyanines via azide-alkyne Huisgen 1,3-dipolar cycloaddition and palladiumcatalyzed Glaser–Hay coupling reactions." Journal of Porphyrins and Phthalocyanines 21, no. 07n08 (2017): 539–46. http://dx.doi.org/10.1142/s108842461750050x.

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In this study, the monomeric subphthalocyanines bearing azido (2) and terminal ethynyl (3) groups were synthesized. These subphthalocyanines were converted to their dimeric derivatives using azide-alkyne Huisgen cycloaddition and palladium-catalyzed Glaser–Hay coupling reactions subphthalocyanine (4) and (5), respectively. The novel subphthalocyanines were fully characterized by elemental analysis and general spectroscopic methods such as MALDI-TOF mass, FT-IR, UV-vis and [Formula: see text]H-NMR. All synthesized subphthalocyanines showed quite good solubility in the most of common organic solvents. The fluorescence measurements were conducted for these subphthalocyanines to estimate their fluorescence quantum yields. The singlet oxygen generation abilities were also examined to investigate their photosensitizer properties.
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Sakamoto, Keiichi, Satoru Yoshino, Makoto Takemoto, et al. "Synthesis of arylsulfanyl-subphthalocyanines and their ring expansion reaction." Journal of Porphyrins and Phthalocyanines 19, no. 05 (2015): 688–94. http://dx.doi.org/10.1142/s1088424615500194.

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For dye-sensitized solar cells, phthalocyanines require strong absorption of far-red light between 700 and 850 nm because of their high electron transfer efficiency. Nevertheless phthalocyanines lack of affinity to basal plats, they inhibit utilization as dye-sensitized solar cell photosensitizer. Then, subphthalocyanines are used as precursors to prepare asymmetric 3:1 type phthalocyanines using a ring-enlargement technique to give affinity to basal plates. As subphthalocyanines having arylsulfanyl substituents used as a precursor, asymmetric phthalocyanines are expected to have good affinity to basal plates. Spectroscopic properties and electron transfer abilities to synthesize non-peripheral arylsulfanyl-subphthalocyanines were estimated. In addition to prepare as trial, asymmetric 3:1 type phthalocyanine, hexakis[(4-methylphenyl)thio]phthalocyanine, was synthesized from corresponding subphthalocyanine.
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Mori, Satoru, Naoya Ogawa, Etsuko Tokunaga, Seiji Tsuzuki, and Norio Shibata. "Design, synthesis and optical properties of unsymmetrical subphthalocyanine trimer connected by phloroglucinol via axial positions." Dalton Transactions 45, no. 3 (2016): 908–12. http://dx.doi.org/10.1039/c5dt04500b.

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Yoshinaga, Kosuke, Leo Delage-Laurin, and Timothy M. Swager. "Fluorous phthalocyanines and subphthalocyanines." Journal of Porphyrins and Phthalocyanines 24, no. 08 (2020): 1074–82. http://dx.doi.org/10.1142/s1088424620500182.

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Incorporating fluorine atoms into a molecule can endow it with various unique properties that enable materials applications. Selective solubility in fluorous solvents is achieved by a high fluorine content and selective partitioning into perfluorinated liquids over organic and aqueous phases provides orthogonal opportunities for chemistry and materials assembly. Although there is a growing number of partially fluorinated molecules, there are insufficient structural design principles to produce diverse fluorous soluble dyes. Herein, we report the synthesis of six fluorous phthalocyanine and subphthalocyanine dyes, and study their properties in the fluorous phase. Phthalocyanines generally display limited solubility and we also observed apparent aggregation in the fluorous phase. However, the nonplanar subphthalocyanines showed greater solubility. Subphthalocyanines also displayed fluorescence in selected solvents, and their emissive properties were investigated. The materials described expand the library of fluorous dyes and provide insights for the design of new molecules with fluorous solubility.
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Shi, Maohu, Jingzhi Chen, and Zhen Shen. "Synthesis and spectroscopic properties of photochromic dithienylethene-functionalized subphthalocyanine conjugate." Journal of Porphyrins and Phthalocyanines 20, no. 08n11 (2016): 1082–89. http://dx.doi.org/10.1142/s108842461650067x.

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A subphthalocyanine-dithienylethene dyad has been synthesized and characterized by 1H-, [Formula: see text]C-NMR, HR-MS, UV-visible and emission spectroscopy. The results show that photoinduced isomerization of dithienylethene moiety from close-form to opened form can be achieved under visible light using subphthalocyanine as a light-harvesting unit and the fluorescence properties of subphthalocyanine could be modulated by the isomerization state of the dithienylethene moiety.
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Trelka, Marta, Anaïs Medina, David Écija, et al. "Subphthalocyanine-based nanocrystals." Chemical Communications 47, no. 36 (2011): 9986. http://dx.doi.org/10.1039/c1cc11658d.

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Morisue, Mitsuhiko, Wataru Suzuki, and Yasuhisa Kuroda. "Hexameric subphthalocyanine rosette." Dalton Transactions 40, no. 39 (2011): 10047. http://dx.doi.org/10.1039/c1dt11214g.

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Shimizu, Soji, Shota Nakano, Takahisa Hosoya, and Nagao Kobayashi. "Pyrene-fused subphthalocyanine." Chem. Commun. 47, no. 1 (2011): 316–18. http://dx.doi.org/10.1039/c0cc01877e.

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Dissertations / Theses on the topic "Subphthalocyanine"

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Garbage, Romain. "Synthèse de nanoroues et de nanovéhicules : exploration des fragments triptycène, subphthalocyanine et bisindénochrysène." Toulouse 3, 2013. http://thesesups.ups-tlse.fr/2081/.

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Du fait de sa symétrie et de sa rigidité, le fragment triptycène est très intéressant à utiliser dans le domaine des nanomachines. Ainsi, il a été utilisé comme roue pour préparer des nanovéhicules mais interagissant trop fortement avec les surfaces d'études, nous avons exploré d'autres fragments en tant que roues moléculaires potentielles. Ces roues moléculaires présentent une structure en bol permettant de diminuer l'interaction avec la surface, augmentant ainsi leur mobilité. De plus, elles possèdent une étiquette permettant de visualiser directement la rotation de la roue par imagerie STM. Ce comportement a été prédit par les études théoriques et observé expérimentalement pour la roue basée sur le fragment subphthalocyanine. La synthèse des roues subphthalocyanine a été réalisée, mais leur connexion via l'atome de bore apical s'est avérée instable sur les surfaces métalliques utilisées. Nous avons donc exploré la synthèse de roues de type bisindenochrysène. Le nanovéhicule à roue triptycène a aussi été étudié sur surface semi-conductrice. Des calculs ont été effectué pour interpréter les images obtenues expérimentalement. Différentes conformations ont été optimisées sur surface semi-conductrice et la conformation la plus stable semble confirmer l'orientation de la molécule sur la surface. Parallèlement à ces recherches sur les nanovéhicules à roues triptycène, nous avons découvert que sur une surface Sm/Si, les triptycènes s'arrangeaient sur les rangées de samarium. Dans le but d'aider à l'auto-organisation unidimensionnelle de ces fragments sur la surface, nous avons synthétisé des dérivés du triptycène fonctionnalisés par des groupes permettant de former des liaisons hydrogène<br>Due to its rigidity and symmetry, very interesting is to use the triptycene fragment in the synthesis of nanomachines. Thus, it has been used as a wheel in nanovehicles but it was found that its interaction with the surface was too strong, so we explored other fragments as new molecular wheel candidates. These new wheels have a bowl-shaped structure in order to decrease the interaction with the surface, improving their mobility. Furthermore, they contain a tag which allows us to directly visualize the rotation of the wheel by STM imaging. This behaviour, which was predicted by theoretical studies was observed experimentally with the subphthalocyanine-based wheel. Subphthalocyanine wheels were synthesized, but it was found that their connexion through the boron atom was unstable on the metallic surfaces used for the STM experiments. This is the reason why we decided to explore the synthesis of wheels based on the bis-indenochrysene fragment. A nanovehicle with four triptycene wheels was also studied on a semiconductor surface. Calculations were carried out in order to interpret the experimental images. Different conformations were optimized on the surface and the most stable conformation seems to confirm the molecule orientation on the surface. In the meantime, it was also discovered that, on Sm/Si surfaces, triptycenes form 1D networks along the samarium rows. In order to promote this 1D organisation, we synthesized functionalized triptycenes capable of self-assembling via hydrogen bonds
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Jacquot, de Rouville Henri-Pierre. "Synthèse de molécules technomimétiques pour des applications en nanomécanique." Toulouse 3, 2010. http://thesesups.ups-tlse.fr/1019/.

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Deux machines moléculaires technomimétiques, dont la forme et la fonction miment des objets macroscopiques, ont été développées au cours de cette thèse : un moteur moléculaire et un nanovéhicule. La première de ces machines est destinée à générer un mouvement de rotation azimutal. C'est une famille de complexes de ruthénium coordinés par un ligand de type scorpionate jouant le rôle de stator et par un ligand pentaphénylcyclopentadiényl jouant le rôle de rotor. Afin de favoriser un mouvement de rotation unidirectionnel du rotor, l'introduction de chiralité a été effectuée dans la structure de la molécule. De plus, un stator fonctionnalisé par un groupement azobenzène et son complexe de ruthénium modèle ont été synthétisés afin d'arrêter de manière contrôlée la rotation du rotor. La seconde machine est quant à elle destinée à générer un mouvement de rotation altitudinal. Pour cela, une nouvelle génération de roues a été élaborée à partir de fragments subphthalocyanine dont la forme de bol ne présente pas d'interactions trop importantes avec la surface. Dès lors, la synthèse d'un nanovéhicule a été envisagée autour d'un plateau polyaromatique<br>Two technomimetic molecular machines, which have the shape and the function of macroscopic objects, were developed during this thesis: a molecular motor and a nanovehicle. The first one was designed in order to control an azimutal rotational motion. This machine is based on a family of ruthenium complexes coordinated by a scorpionate ligand acting as a stator and a pentaphenylcyclopentadienyl ligand acting as a rotor. In order to favor a unidirectional rotation of the rotor, introduction of chirality was achieved in the design of the molecule. Besides, a stator functionalized with an azobenzene functional group and its ruthenium model complex were synthesized in order to lock the rotation of the rotor in a controlled manner. The second machine was designed to control an altitudinal rotational motion. To achieve this goal, a new generation of wheels was synthesised based on subphthalocyanine fragments which have a bowl shape structure avoiding too many interactions with the surface. The synthesis of a nanovehicle was considered around a polyaromatic core
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Glebe, Ulrich [Verfasser]. "Selbstassemblierte Monolagen und magnetisch strukturierte Submonolagen mit dia- und paramagnetischen Molekülen sowie Einzelmolekülmagneten auf Phthalocyanin- und Subphthalocyanin-Basis / Ulrich Glebe." Kassel : Universitätsbibliothek Kassel, 2012. http://d-nb.info/1018927565/34.

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阿久斗, 髙木, 高木 阿久斗 та Akuto Takagi. "有機半導体材料の開発 : 共役系骨格に対する置換基導入の集積性への影響とデバイス応用に向けた物性評価". Thesis, https://doors.doshisha.ac.jp/opac/opac_link/bibid/BB13071699/?lang=0, 2018. https://doors.doshisha.ac.jp/opac/opac_link/bibid/BB13071699/?lang=0.

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Ebenhoch, Bernd. "Organic solar cells : novel materials, charge transport and plasmonic studies." Thesis, University of St Andrews, 2015. http://hdl.handle.net/10023/7814.

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Organic solar cells have great potential for cost-effective and large area electricity production, but their applicability is limited by the relatively low efficiency. In this dissertation I report investigations of novel materials and the underlying principles of organic solar cells, carried out at the University of St Andrews between 2011 and 2015. Key results of this investigation: • The charge carrier mobility of organic semiconductors in the active layer of polymer solar cells has a rather small influence on the power conversion efficiency. Cooling solar cells of the polymer:fullerene blend PTB7:PC₇₁BM from room temperature to 77 K decreased the hole mobility by a factor of thousand but the device efficiency only halved. • Subphthalocyanine molecules, which are commonly used as electron donor materials in vacuum-deposited active layers of organic solar cells, can, by a slight structural modification, also be used as efficient electron acceptor materials in solution-deposited active layers. Additionally these acceptors offer, compared to standard fullerene acceptors,advantages of a stronger light absorption at the peak of the solar spectrum. • A low band-gap polymer donor material requires a careful selection of the acceptor material in order to achieve efficient charge separation and a maximum open circuit voltage. • Metal structures in nanometer-size can efficiently enhance the electric field and light absorption in organic semiconductors by plasmonic resonance. The fluorescence of a P3HT polymer film above silver nanowires, separated by PEDOT:PSS, increased by factor of two. This could be clearly assigned to an enhanced absorption as the radiative transition of P3HT was identical beside the nanowires. • The use of a processing additive in the casting solution for the active layer of organic solar cells of PTB7:PC₇₁BM strongly influences the morphology, which leads not only to an optimum of charge separation but also to optimal charge collection.
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Menting, Raoul. "Light-induced energy and charge transfer processes in artificial photosynthetic systems." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2013. http://dx.doi.org/10.18452/16656.

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Der Gegenstand der vorliegenden Arbeit ist die Untersuchung von photoinduzierten Energietransferprozessen (EET) und Elektronentransferprozessen (ET) in Modellsystemen, die als potentiell geeignet für eine Nutzung in der artifiziellen Photosynthese angesehen werden. Den beiden wesentlichen Zugängen zur Architektur artifizieller Photosynthese-Systeme entsprechend wurden vergleichend kovalente und sich selbst organisierende Systeme untersucht. In beiden Zugängen wurden ähnliche chemische Komponenten als optisch aktive Moleküle eingesetzt, insbesondere Phthalocyanine mit einem Silizium-Zentralatom (SiPc). Durch eine Kombination von stationären und zeitaufgelösten optisch-spektroskopischen Methoden konnten die lichtinduzierten ET- und EET-Prozesse identifiziert und quantifiziert werden. Im ersten Teil der Arbeit wurden mehrere kovalent gebundene Triaden und eine Pentade untersucht. In allen Systemen finden sehr effiziente ET und EET Prozesse statt. Es wurde gezeigt, dass das Lösungsmittel großen Einfluss auf die photophysikalischen Eigenschaften der Systeme ausübt. Die Lebensdauer des ladungsseparierten Zustandes variiert von 1,7 ns in Toluol bis 30 ps in DMF. Im zweiten Teil der Arbeit wurde erstmals gezeigt, dass sich in wässriger Lösung ein supramolekularer Komplex, bestehend aus einem Beta-Cyklodextrin (CD), einem konjugierten Subphthylocyanin (SubPc), einem Porphyrin (Por) und einem SiPc bilden kann. Letzteres wurde über unterschiedliche Ketten an zwei CDs kovalent gebunden. Die Selbstorganisation wird über hydrophobe Wechselwirkungen vermittelt und die Bildung der Komplexe ist sehr effizient. Nach selektiver Anregung von SubPc finden sequenzielle ET- und EET-Prozesse von SubPc zu SiPc statt. Das Por spielt die Rolle einer energetischen und elektronischen Brücke und ermöglicht die ET und EET-Prozesse von SubPc zu SiPc. Die Ladungsrekombination in den Grundzustand geschieht innerhalb von 1,7 ns.<br>The main objective of the present thesis was to conduct investigations of photo-induced electron transfer (ET) and excitation energy transfer (EET) processes in model compounds that are considered potentially appropriate for use in artificial photosynthesis. Two approaches have been used to construct the artificial photosynthetic systems, namely covalent and supramolecular approach. In both systems similar optically active molecules have been employed, particularly silicon-based phthalocyanines (SiPc). A comparative study between the covalently-linked and self-assembled systems had been conducted. For these purposes, thorough spectroscopic measurements in the UV/Vis range had been performed on these conjugates. A combination of steady-state and time-resolved experiments allowed an identification and quantification of the photo-induced ET and EET processes. In the first part of the work several covalently bound triads and a pentad bearing a central SiPc unit were studied. In all systems highly efficient ET and EET processes take place. It was found that the solvent exerts great influence on the photophysical properties of the systems. The lifetime of the charge-separated state varied from 1.7 ns (toluene) down to 30 ps (DMF). In the second part of the thesis, for the first time the formation of ternary supramolecular complexes consisting of a beta-cyclodextrin (CD), a conjugated subphthalocyanine (SubPc), a porphyrin (Por) and a series of SiPcs substituted axially with two CDs via different spacers was shown. These components are held in water by host-guest interactions and the formation of these host-guest complexes was found to be very efficient. Upon excitation of the SubPc-part of the complex sequential ET and EET processes from SubPc to SiPc take place. The Por dye acts as a transfer bridge enabling these processes. The probability of ET is controlled by the linker between CD and SiPc. Charge recombination to the ground state occurs within 1.7 ns.
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Eder, Grace M. "Dye Molecule-Based Porous Organic Materials." The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1530012900215452.

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Bernhard, Yann. "Synthèse et étude de nouvelles sondes fluorescentes pour l'imagerie optique, l'imagerie Cherenkov et les imageries multimodales." Thesis, Dijon, 2015. http://www.theses.fr/2015DIJOS015/document.

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Le travail présenté dans ce mémoire avait pour but d’étudier le potentiel de nouvelles sondes fluorescentes pour la mise au point d’agents d’imagerie optique et d’imagerie Cherenkov inédits. Le premier chapitre porte sur la synthèse de subphtalocyanines et phtalocyanines fluorescentes possédant des fonctions chimiques qui confèrent à la molécule des propriétés adaptées à une application en imagerie médicale. Les composés obtenus ont été étudiés pour déterminer s’ils possèdent les propriétés requises pour l’application visée, en considération du cahier des charges propre aux fluorophores. Dans un deuxième temps, certaines sondes fonctionnelles préparées ont été utilisées pour créer des agents d’imagerie inédits. Dans le cas des subphtalocyanines, la biovectorisation a été explorée par association directe de la sonde avec un peptide, ou indirecte grace à un liposome encapsulant la sonde. Dans le cas des phtalocyanines, les sondes fonctionnelles ont été engagées dans la préparation de nanohybrides constitués de nanoparticules d’oxyde de fer ou de nanotubes d’oxyde de titane, afin d’obtenir des agents bimodaux ou théranostiques. Le troisième chapitre présente l’étude du phénomène de transfert d’énergie (CRET) entre des radioéléments émetteurs Cherenkov et des fluorophores organiques a été étudié. La détermination des paramètres de transfert optimaux a ensuite guidé la mise au point d’une sonde CRET composée d’un fragment fluorescéine lié covalentement à un complexe d’yttrium-90. Pour finir, la possibilité d’émettre dans la fenêtre du proche infrarouge a été explorée par multi-transfert de type CRETFRET<br>The goal of this work was to prepare and study new fluorescent probes, which could give rise to novel optical or Cherenkov imaging agents. The first section of this work describes the synthesis of fluorescent subphthalocyanines and phthalocyanines probes, which possess relevant chemicals groups suitable for optical imaging applications. The optical and physico-chemical properties of the new probes were carefully examined to ensure they comply with the specification of the fluorophores for the desired application. The second part focused on the subsequent development of a few selected probes into real imaging agents. The biovectorisation of subphtalocyanines was achieved upon conjugation of a peptide either with the probe or with a liposome that encapsulate the probe. Phthalocyanine-based functional probes were engaged in the synthesis of nanohybrides made of iron oxide nanoparticles or titania nanotubes, to afford bimodal or theranostic agents. In a final part, the energy transfer phenomenon (CRET) between Cherenkov emitting radionuclides and organic fluorophores was studied. The optimal transfer parameters were considered to prepare a CRET probe made of a fluorescein moiety covalently attached to an Yttrium-90 complex. Finally, the ability to emit in the near infrared window was explored by multi-CRET-FRET transfer
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Brisson, Emma. "Stable Boron Subphthalocyanines: A Structure Property Relationship and New Processes for Further Synthetic Study." Thesis, 2011. http://hdl.handle.net/1807/30523.

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A structure property relationship relating photostability with the axial and peripheral substituents of Boronsubphthalocyanine (BsubPc) derivatives has been outlined: peripherally halogenating BsubPc has been determined to be the best way to increase the photostability, while axial substituents are found to have little effect. A solid state photostability test using BsubPc doped polymer films has been developed and was used to form this structure property relationship. The polymer in which BsubPc is tested is found to have an effect on the photostability and should be further explored. In addition to the structure property relationship, processes to make new BsubPc precursors, HO-BsubPc and Br-BsubPc, have been developed in order to further expand the derivatives available for study.
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Morse, Graham Edward Jr. "Engineering Boronsubphthalocyanine for Organic Electronic Applications." Thesis, 2012. http://hdl.handle.net/1807/35083.

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Boronsubphthalocyanines (BsubPcs) are a class of organic semiconducting materials which are relatively underdeveloped in their synthetic methods and organic semiconducting applications. A comprehensive investigation of these materials is explored in a rigorous and strategic manner progressing through each stage of the materials development cycle: materials selection from computational screening, organic/organometallic synthesis of target materials using known methods or by the development of new synthetic methods, physical and chemical analysis of new materials, and device implementation in organic light emitting diodes and organic photovoltaic cells. The result is the formation of new compositions of BsubPc specifically engineered for application as organic semiconductors in devices. Specifically, phenoxy-boronsubphthalocyanine derivatives are investigated starting with a computational study of their molecular orbitals – a property that dictates their function (donor or acceptor behaviour) in organic electronic devices. The nature of the axial phenoxylate is found to vary the energy level of the frontier molecular orbitals minimally, by up to ~0.4 eV while the nature of the BsubPc periphery can shift the energy levels of the frontier molecular orbitals by >1 eV. The differential sensitivity of the axial phenoxylate and the BsubPc periphery becomes a key design element allowing controlled adjustments of the frontier molecular orbitals by peripheral modification and isolating the design physical chemical properties essential to device fabrication to the axial phenoxylate. Subsequently, an investigation into the solubility and sublimability of these materials is performed, which leads to their investigation in OLED and OPV devices. The success from the phenoxy-BsubPcs study has led to the exploration of new chemistry to expand the available axial nucleophiles beyond phenoxylates. Previously unattainable sulphur and nitrogen nucleophiles are synthesised using two methods (1) the condensation of Cl-BsubPc with phthalimides and (2) the activation of Cl-BsubPc using aluminum chloride to access thiols and anilines. The phthalimido-BsubPcs synthesized from this method are incorporated in OLEDs.
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Book chapters on the topic "Subphthalocyanine"

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Jacquot de Rouville, Henri-Pierre, Romain Garbage, Agnès M. Sirven, Claire Kammerer, and Gwénaël Rapenne. "Triptycene or Subphthalocyanine Wheels and Polyaromatic Hydrocarbon Nanovehicles." In Single Molecular Machines and Motors. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-13872-5_4.

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Claessens, Christian G., Gema de la Torre, and Tomás Torres. "From Dipolar to Octupolar Phthalocyanine Derivatives: The Example of Subphthalocyanines." In Challenges and Advances in Computational Chemistry and Physics. Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4850-5_16.

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L. Pakhomov, Georgy, Vlad V. Travkin, and Pavel A. Stuzhin. "Hexachlorinated Boron(III) Subphthalocyanine as Acceptor for Organic Photovoltaics: A Brief Overview." In Recent Advances in Boron-Containing Materials. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.90292.

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McKeown, N. B. "Subphthalocyanines." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01937.

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Yurt, Fatma, Kasim Ocakoglu, Ozge Er, et al. "Evaluation of photodynamic therapy and nuclear imaging potential of subphthalocyanine integrated TiO2 nanoparticles in mammary and cervical tumor cells." In Porphyrin Science by Women. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811223556_0024.

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McKeown, N. B. "Trisubstituted Subphthalocyanines from Phthalonitriles." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01939.

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McKeown, N. B. "Hexasubstituted Subphthalocyanines from Phthalonitriles." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01940.

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"2. Phthalocyanines and Related Compounds: 2.2. Synthesis of Subphthalocyanines." In Hetarenes IV, edited by Ernst Schaumann. Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-111052.

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McKeown, N. B. "AAAB-Type Phthalocyanines from the Ring Expansion of Subphthalocyanines." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01950.

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Sgobba, Vito, and Dirk M. Guldi. "Nanohybrids Based on Porphyrins, Phthalocyanines and Subphthalocyanines in Combination with Graphene and Related Materials: New Developments." In Handbook of Porphyrin Science (Volumes 36 – 40). World Scientific Publishing Company, 2016. http://dx.doi.org/10.1142/9789813149601_0001.

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Conference papers on the topic "Subphthalocyanine"

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Wang, Yang, Donghong Gu, and Fuxi Gan. "Application of subphthalocyanine thin films in high-density optical recording." In Optical Storage (ISOS 2002), edited by Fuxi Gan and Zuoyi Li. SPIE, 2003. http://dx.doi.org/10.1117/12.510077.

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Zang, Yue, Jungsheng Yu, Jiang Huang, and Yadong Jiang. "Charge carrier losses of organic solar cells based on subphthalocyanine/C60heterojunction." In 6th International Symposium on Advanced Optical Manufacturing and Testing Technologies (AOMATT 2012), edited by Yadong Jiang, Junsheng Yu, and Zhifeng Wang. SPIE, 2012. http://dx.doi.org/10.1117/12.977837.

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Ma, Biwu, Yoshikazu Miyamoto, Claire H. Woo, Jean M. J. Fréchet, Fan Zhang, and Yi Liu. "Solution processable boron subphthalocyanine derivatives as active materials for organic photovoltaics." In SPIE Photonic Devices + Applications, edited by Zakya H. Kafafi and Paul A. Lane. SPIE, 2009. http://dx.doi.org/10.1117/12.825372.

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Wang, Po-Sheng, Cheng-Chieh Lee, Jiun-Haw Lee, Lee-Yih Wang, Chi-Feng Lin, and Tien-Lung Chiu. "Boron subphthalocyanine-based organic photovoltaic device with record high open circuit voltage." In 2015 22nd International Workshop on Active-Matrix Flatpanel Displays and Devices (AM-FPD). IEEE, 2015. http://dx.doi.org/10.1109/am-fpd.2015.7173236.

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Durantini, Edgardo, and Mariana Spesia. "Synthesis of a tricationic subphthalocyanine with potential use in photoinactivation of bacteria." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01393.

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Ma, Zhu, Junsheng Yu, Juan Zhao, Shengqiang Liu, and Longfeng Jiang. "Metallophthalocyanine and subphthalocyanine films as electron-transport layer in organic light-emitting diodes." In 6th International Symposium on Advanced Optical Manufacturing and Testing Technologies (AOMATT 2012), edited by Yadong Jiang, Junsheng Yu, and Zhifeng Wang. SPIE, 2012. http://dx.doi.org/10.1117/12.978655.

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Wang, Yang, Donghong Gu, and Fuxi Gan. "Spectral and optical properties of a new subphthalocyanine dye as a potential optical recording material." In Fifth International Symposium on Optical Storage (IS0S 2000), edited by Fuxi Gan and Lisong Hou. SPIE, 2001. http://dx.doi.org/10.1117/12.416832.

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Hao, X., S. Wang, T. Sakurai, and K. Akimoto. "The Effect of Bathocuproine (BCP) buffer layer in boron subphthalocyanine chloride (SubPc)/fullerene (C60) Organic Solar Cells with inverted structure." In 2014 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2014. http://dx.doi.org/10.7567/ssdm.2014.k-3-4.

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Lilichenko, Nadezda, Robert Ossig, Ulrich Glebe, Ulrich Siemeling, Frank Hubenthal, and Frank Träger. "SHG studies of self-assembled monolayers of subphthalocyanines on gold." In SPIE LASE, edited by Jan J. Dubowski, David B. Geohegan, and Frank Träger. SPIE, 2013. http://dx.doi.org/10.1117/12.2001277.

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Zasedatelev, A. V., T. V. Dubinina, V. I. Krasovskii, and A. B. Karpo. "Strong saturable-absorption effect in subphthalocyanines caused by plasmonic nanoparticles." In 2016 International Conference Laser Optics (LO). IEEE, 2016. http://dx.doi.org/10.1109/lo.2016.7549873.

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