Relevant bibliographies by topics / TRIAZOLO-TRIAZINE

Contents

  1. Journal articles
  2. Book chapters

Academic literature on the topic 'TRIAZOLO-TRIAZINE'

Author: Grafiati
Published: 1 April 2023

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 'TRIAZOLO-TRIAZINE.'

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 "TRIAZOLO-TRIAZINE"

1

Wang, Qian, Yanli Shao, and Ming Lu. "Amino-tetrazole functionalized fused triazolo-triazine and tetrazolo-triazine energetic materials." Chemical Communications 55, no. 43 (2019): 6062–65. http://dx.doi.org/10.1039/c9cc01777a.

Full text
Abstract:
In this study, two insensitive energetic compounds using fused triazolo-triazine and tetrazolo-triazine as the framework, one amino and one tetrazole as functional groups, were prepared through a two-step reaction.
APA, Harvard, Vancouver, ISO, and other styles
2

Pathak, Suraj Kumar, Yepeng Xiang, Manli Huang, Taian Huang, Xiaosong Cao, He Liu, Guohua Xie, and Chuluo Yang. "Fused tetracyclic tris[1,2,4]triazolo[1,3,5]triazine as a novel rigid electron acceptor for efficient thermally activated delayed fluorescence emitters." RSC Advances 10, no. 26 (2020): 15523–29. http://dx.doi.org/10.1039/d0ra01925a.

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

Zeng, Qun, Yanyang Qu, Jinshan Li, and Hui Huang. "Theoretical studies on the derivatives of tris([1,2,4]triazolo)[4,3-a:4′,3′-c:4′′,3′′-e][1,3,5]triazine as high energetic compounds." RSC Advances 6, no. 7 (2016): 5419–27. http://dx.doi.org/10.1039/c5ra22524h.

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

Navarro, Amparo, M. Paz Fernández-Liencres, Gregorio García, José M. Granadino-Roldán, and Manuel Fernández-Gómez. "A DFT approach to the charge transport related properties in columnar stacked π-conjugated N-heterocycle cores including electron donor and acceptor units." Physical Chemistry Chemical Physics 17, no. 1 (2015): 605–18. http://dx.doi.org/10.1039/c4cp04220d.

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

Bernat, Zofia, Anna Szymanowska, Mateusz Kciuk, Katarzyna Kotwica-Mojzych, and Mariusz Mojzych. "Review of the Synthesis and Anticancer Properties of Pyrazolo[4,3-e][1,2,4]triazine Derivatives." Molecules 25, no. 17 (August 29, 2020): 3948. http://dx.doi.org/10.3390/molecules25173948.

Full text
Abstract:
This review focuses on the cytotoxic effect of new synthetic pyrazolo[4,3-e][1,2,4]triazine derivatives against different tumor cell lines. Some annulated pyrazolotriazines i.e., pyrazolo[4,3-e][1,2,4]triazolo[4,3-b][1,2,4]triazines and pyrazolo[4,3-e]tetrazolo[1,5-b][1,2,4]triazine demonstrated significant broad cytotoxic activity in micromolar range concentration, which could have excellent potential to be new candidate therapeutic agents in cancer chemotherapy.
APA, Harvard, Vancouver, ISO, and other styles
6

Hojo, Ryoga, Don M. Mayder, and Zachary M. Hudson. "Donor–acceptor materials exhibiting deep blue emission and thermally activated delayed fluorescence with tris(triazolo)triazine." Journal of Materials Chemistry C 9, no. 40 (2021): 14342–50. http://dx.doi.org/10.1039/d1tc03480d.

Full text
Abstract:
Five emitters with the tris(triazolo)triazine acceptor core are reported, with emission from deep blue to green. These emitters show promising thermally activated delayed fluorescence and/or two-photon fluorescence properties.
APA, Harvard, Vancouver, ISO, and other styles
7

Hojo, Ryoga, Don M. Mayder, and Zachary M. Hudson. "Donor–acceptor materials exhibiting deep blue emission and thermally activated delayed fluorescence with tris(triazolo)triazine." Journal of Materials Chemistry C 9, no. 40 (2021): 14342–50. http://dx.doi.org/10.1039/d1tc03480d.

Full text
Abstract:
Five emitters with the tris(triazolo)triazine acceptor core are reported, with emission from deep blue to green. These emitters show promising thermally activated delayed fluorescence and/or two-photon fluorescence properties.
APA, Harvard, Vancouver, ISO, and other styles
8

Hundemer, Fabian, Ettore Crovini, Yoshimasa Wada, Hironori Kaji, Stefan Bräse, and Eli Zysman-Colman. "Tris(triazolo)triazine-based emitters for solution-processed blue thermally activated delayed fluorescence organic light-emitting diodes." Materials Advances 1, no. 8 (2020): 2862–71. http://dx.doi.org/10.1039/d0ma00659a.

Full text
Abstract:
We report a new emitter 3,4,5-3TCz-TTT based on a tris(triazolo)triazine acceptor that shows thermally activated delayed fluorescence and cross-compare its performance with the recently reported analogue, 3DMAC-TTT.
APA, Harvard, Vancouver, ISO, and other styles
9

Fang, Zhou, Shengyue Wang, Junxu Liao, Xinrui Chen, Yuanyuan Zhu, Weiguo Zhu, and Yafei Wang. "Asymmetric sky-blue thermally-activated delayed fluorescence emitters bearing tris(triazolo)triazine moiety for solution-processable organic light-emitting diodes." Journal of Materials Chemistry C 10, no. 12 (2022): 4837–44. http://dx.doi.org/10.1039/d1tc05372h.

Full text
Abstract:
Two sky-blue TADF emitters bearing the tris(triazolo)triazine acceptor moiety were designed and synthesized. The solution-processed OLEDs based on these two emitters achieved a maximum EQE of 10.01% at 474 nm.
APA, Harvard, Vancouver, ISO, and other styles
10

Anikin, Oleg V., Nikita E. Leonov, Michael S. Klenov, Aleksandr M. Churakov, Alexey A. Voronin, Nikita V. Muravyev, Yurii A. Strelenko, Ivan V. Fedyanin, and Vladimir A. Tartakovsky. "An Energetic (Nitro-NNO -azoxy)triazolo-1,2,4-triazine." European Journal of Organic Chemistry 2019, no. 26 (June 13, 2019): 4189–95. http://dx.doi.org/10.1002/ejoc.201900314.

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

Book chapters on the topic "TRIAZOLO-TRIAZINE"

1

Lindsley, C. W., and M. E. Layton. "Synthesis of [1,2,3]Triazolo[5,1-][1,2,4]triazine." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00583.

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

Lindsley, C. W., and M. E. Layton. "Synthesis of 1,2,4-Triazolo[3,4-][1,2,4]triazine 7-Oxide." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00605.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'TRIAZOLO-TRIAZINE' for particular source types:
Journal articles
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