Relevant bibliographies by topics / Hexaphyrins

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Hexaphyrins'

Author: Grafiati
Published: 24 May 2025
Last updated: 31 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Hexaphyrins.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Hexaphyrins"

1

Mori, Hirotaka, Masaaki Suzuki, Woojae Kim, Jong Min Lim, Dongho Kim та Atsuhiro Osuka. "5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents". Chemical Science 6, № 3 (2015): 1696–700. http://dx.doi.org/10.1039/c4sc03394a.

Full text
Abstract:
A series of [26]hexaphyrins(1.1.1.1.1.1) bearing two α-oligothienyl substituents at 5,20-positions have been synthesised and are shown to have a dumbbell hexaphyrin conformation, to which the α-oligothienyl groups are linked to form an acyclic helix-like conjugated network.
APA, Harvard, Vancouver, ISO, and other styles
2

Lopes, Susana M. M., Marta Pineiro, and Teresa M. V. D. Pinho e Melo. "Corroles and Hexaphyrins: Synthesis and Application in Cancer Photodynamic Therapy." Molecules 25, no. 15 (2020): 3450. http://dx.doi.org/10.3390/molecules25153450.

Full text
Abstract:
Corroles and hexaphyrins are porphyrinoids with great potential for diverse applications. Like porphyrins, many of their applications are based on their unique capability to interact with light, i.e., based on their photophysical properties. Corroles have intense absorptions in the low-energy region of the uv-vis, while hexaphyrins have the capability to absorb light in the near-infrared (NIR) region, presenting photophysical features which are complementary to those of porphyrins. Despite the increasing interest in corroles and hexaphyrins in recent years, the full potential of both classes o
APA, Harvard, Vancouver, ISO, and other styles
3

Sinha, Avisikta, and Mangalampalli Ravikanth. "Phenothiazine-Embedded Hexaphyrins." Organic Letters 24, no. 6 (2022): 1335–40. http://dx.doi.org/10.1021/acs.orglett.1c04374.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Yadav, Bharti, and Mangalampalli Ravikanth. "Bis-(Fluorene)-Embedded Hexaphyrins." Journal of Organic Chemistry 87, no. 5 (2022): 2543–50. http://dx.doi.org/10.1021/acs.joc.1c02488.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Suzuki, Masaaki, and Atsuhiro Osuka. "Cross-Bridging Reaction of 5,20-Diethynyl Substituted Hexaphyrins to Vinylene-Bridged Hexaphyrins." Journal of the American Chemical Society 129, no. 3 (2007): 464–65. http://dx.doi.org/10.1021/ja067102v.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Rath, Harapriya, Naoki Aratani, Jong Min Lim, et al. "Bis-rhodium hexaphyrins: metalation of [28]hexaphyrin and a smooth Hückel aromatic–antiaromatic interconversion." Chemical Communications, no. 25 (2009): 3762. http://dx.doi.org/10.1039/b905859a.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Lim, Jong Min, Karthik Ganesan, Young Mo Sung, Alagar Srinivasan, Tavarekere K. Chandrashekar, and Dongho Kim. "Photophysical properties of bridged core-modified hexaphyrins: conjugational perturbation of thiophene bridges." Chem. Commun. 50, no. 33 (2014): 4358–60. http://dx.doi.org/10.1039/c4cc00309h.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Fliegl, Heike, Dage Sundholm, Stefan Taubert, and Fabio Pichierri. "Aromatic Pathways in Twisted Hexaphyrins." Journal of Physical Chemistry A 114, no. 26 (2010): 7153–61. http://dx.doi.org/10.1021/jp1021517.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Oh, Juwon, Hirotaka Mori, Young Mo Sung, Woojae Kim, Atsuhiro Osuka та Dongho Kim. "Switchable π-electronic network of bis(α-oligothienyl)-substituted hexaphyrins between helical versus rectangular circuit". Chemical Science 7, № 3 (2016): 2239–45. http://dx.doi.org/10.1039/c5sc04263a.

Full text
Abstract:
The switching phenomena of conformation with π-electronic network through deprotonation–protonation processes were investigated by employing a series of 5,20-bis(α-oligothienyl) substituted hexaphyrins(1.1.1.1.1.1).
APA, Harvard, Vancouver, ISO, and other styles
10

Higashino, Tomohiro, Mitsunori Inoue, and Atsuhiro Osuka. "SinglyN-Fused Möbius Aromatic [28]Hexaphyrins(1.1.1.1.1.1)." Journal of Organic Chemistry 75, no. 22 (2010): 7958–61. http://dx.doi.org/10.1021/jo1018156.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Hexaphyrins"

1

Koide, Taro. "Studies on Open-shell Hexaphyrins." 京都大学 (Kyoto University), 2012. http://hdl.handle.net/2433/157798.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Inoue, Mitsunori. "Studies on Möbius Aromaticity of Hexaphyrins." 京都大学 (Kyoto University), 2011. http://hdl.handle.net/2433/142391.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Suzuki, Masaaki. "Chemistry of meso-aryl substituted hexaphyrins(1.1.1.1.1.1)." 京都大学 (Kyoto University), 2007. http://hdl.handle.net/2433/136786.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Khrueawatthanawet, Thanaphon. "Synthesis of cyclodextrin-hexaphyrin hybrids en route to unorthodox π-type (anti)aromatic interaction receptors". Electronic Thesis or Diss., Sorbonne université, 2024. http://www.theses.fr/2024SORUS522.

Full text
Abstract:
Contrairement à l'aromaticité de Hückel classique, peu de choses sont connues sur les aromaticités dites « non orthodoxes » (c'est-à-dire l'antiaromaticité de Hückel et l'aromaticité de Möbius) en raison de leur totale absence dans la nature et de la difficulté à les synthétiser. Par conséquent, peu d'études ont été menées pour explorer les interactions de type π impliquant ces aromaticities non orthodoxes. Cependant, ces caractéristiques se retrouvent dans la famille des dérivés porphyrinoïdes, en particulier les hexaphyrines, qui peuvent alternativement adopter un caractère Hückel antiaromat
APA, Harvard, Vancouver, ISO, and other styles
5

Mori, Shigeki. "Studies on metallation of meso-aryl substituted hexaphyrins and N-fused pentaphyrins." 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/136922.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Ruffin, Hervé. "Influence d'un habillage sur les propriétés de coordination d'hexaphyrines : vers des nouveaux récepteurs moléculaires à conformation et aromaticité modulables." Thesis, Rennes 1, 2017. http://www.theses.fr/2017REN1S086/document.

Full text
Abstract:
Les hexaphyrines sont des macrocycles constitués de six unités pyrroliques, elles possèdent des propriétés physico-chimiques intéressantes, dont notamment leur capacité à exister sous deux états oxydés stables, à 26 et 28 électrons π délocalisés. Elles peuvent coordonner jusqu’à deux cations métalliques au sein du macrocycle, cependant elles souffrent d’un manque de réactivité et de prédictibilité quant à la nature des complexes formés. Pour pallier à ces problèmes, nous avons décidé de suivre une stratégie de post-modification du macrocycle, mettant en jeu l’incorporation sans précédent d’un
APA, Harvard, Vancouver, ISO, and other styles
7

Benchouaïa, Rajaa. "Vers de nouveaux métallo-récepteurs : synthèse et études de ligands hybrides hexaphyrine-cyclodextrine." Thesis, Rennes 1, 2019. http://www.theses.fr/2019REN1S116.

Full text
Abstract:
Les hexaphyrines sont constituées de six unités pyrroliques et présentent différents types d'aromaticité, à l'origine de leurs remarquables propriétés de coordination. Cependant, les complexes sont décrits majoritairement sur des hexaphyrines « nues ». De plus, l'induction de chiralité sur un anneau de Möbius n'en est qu'à ses prémices. Dans ce contexte, nous explorons les propriétés de coordination des hexaphyrines « chapeautées ». Plus particulièrement, notre objectif consiste à élaborer des ligands hybrides, dont les unités hexaphyrine et cyclodextrine sont liées de manières covalentes. Pou
APA, Harvard, Vancouver, ISO, and other styles
8

Mori, Goro, Hiroshi Shinokubo, and Atsuhiro Osuka. "Highly selective Ir-catalyzed direct sixfold borylation of peripheral aromatic substituents on hexakisaryl-substituted [28]hexaphyrin(1.1.1.1.1.1)." Elsevier, 2008. http://hdl.handle.net/2237/12313.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Yoneda, Tomoki. "Novel π-Conjugation Circuits and Coordination Structures of Metalated Expanded Porphyrins". 京都大学 (Kyoto University), 2015. http://hdl.handle.net/2433/199132.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Naoda, Koji. "Study on Metalated and Cross-Conjugated Expanded Porphyrins." 京都大学 (Kyoto University), 2017. http://hdl.handle.net/2433/225425.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Hexaphyrins"

1

Gautam, Anshu, Poonam Rawat, and R. N. Singh. "DIPYRROMETHANE, ITS DERIVATIVES AND THEIR METAL COMPLEX: APPLICATIONS AS CHEMOSENSORS AND BIOLOGICAL ACTIVITY." In Futuristic Trends in Chemical Material Sciences & Nano Technology Volume 3 Book 20. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3becs20p1ch5.

Full text
Abstract:
Pyrrole moiety forms many naturally occurring biologically active compounds and exist in the structure of some biologically active compounds. From this point of view, pyrrole derivatives are very important building blocks in the drug industry and so in organic syntheses. Dipyrromethane derivatives are the building blocks for the syntheses of a variety of calix[n]pyrroles, porphyrins, hexaphyrin and polypyrrolicmacrocycles. The oxidized dipyrromethane derivatives (i.e. dipyrromethenes or dipyrrins) have strong coordinating ability towards different metal ions and their metal complexes with triv
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Hexaphyrins' for particular source types:
Journal articles Dissertations / Theses
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography