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Journal articles on the topic 'Tribranched'

Author: Grafiati

Published: 9 March 2023

Last updated: 31 July 2025

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1

He, Guiying, Jinjun Shao, Yang Li, et al. "Photophysical properties of octupolar triazatruxene-based chromophores." Physical Chemistry Chemical Physics 18, no. 9 (2016): 6789–98. http://dx.doi.org/10.1039/c5cp07563g.

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2

Suzuki, Akira, Munetaka Akita, and Michito Yoshizawa. "Amphiphilic tribranched scaffolds with polyaromatic panels that wrap perylene stacks displaying unusual emissions." Chemical Communications 52, no. 65 (2016): 10024–27. http://dx.doi.org/10.1039/c6cc04823d.

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A spherical assembly containing a perylene stack, prepared from a rigid tribranched scaffold and perylene, exhibits unusual Y-emission in water at room temperature. In contrast, an analogous assembly from a flexible scaffold and perylene shows E-emission under the same conditions.

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3

Zhang, Ji-Na, Hong Li, Wei Zhou, Shi-Lin Yu, Da-Hui Qu, and He Tian. "Fluorescence Modulation in Tribranched Switchable [4]Rotaxanes." Chemistry - A European Journal 19, no. 50 (2013): 17192–200. http://dx.doi.org/10.1002/chem.201303026.

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4

Tateishi-Karimata, Hisae, Tatsuya Ohyama, Takahiro Muraoka, Shigenori Tanaka, Kazushi Kinbara, and Naoki Sugimoto. "New Modified Deoxythymine with Dibranched Tetraethylene Glycol Stabilizes G-Quadruplex Structures." Molecules 25, no. 3 (2020): 705. http://dx.doi.org/10.3390/molecules25030705.

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Methods for stabilizing G-quadruplex formation is a promising therapeutic approach for cancer treatment and other biomedical applications because stable G-quadruplexes efficiently inhibit biological reactions. Oligo and polyethylene glycols are promising biocompatible compounds, and we have shown that linear oligoethylene glycols can stabilize G-quadruplexes. Here, we developed a new modified deoxythymine with dibranched or tribranched tetraethylene glycol (TEG) and incorporated these TEG-modified deoxythymines into a loop region that forms an antiparallel G-quadruplex. We analyzed the stabili

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5

VALLE, Cristina. "On the blow-analytic equivalence of tribranched plane curves." Journal of the Mathematical Society of Japan 68, no. 2 (2016): 823–38. http://dx.doi.org/10.2969/jmsj/06820823.

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6

Friedl, Stefan, Takahiro Kitayama, and Matthias Nagel. "A note on the existence of essential tribranched surfaces." Topology and its Applications 225 (July 2017): 75–82. http://dx.doi.org/10.1016/j.topol.2017.04.023.

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7

Lee, Geon Hyeong, and Young Sik Kim. "Theoretical study of tribranched organic sensitizer for Efficient Dye-sensitized solar cells." Molecular Crystals and Liquid Crystals 653, no. 1 (2017): 260–66. http://dx.doi.org/10.1080/15421406.2017.1354654.

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8

Zhu, Lin, Wen Lv, Shujuan Liu, Hong Yan, Qiang Zhao, and Wei Huang. "Carborane enhanced two-photon absorption of tribranched fluorophores for fluorescence microscopy imaging." Chemical Communications 49, no. 90 (2013): 10638. http://dx.doi.org/10.1039/c3cc46276e.

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9

Abbotto, Alessandro, Valentina Leandri, Norberto Manfredi, et al. "Bis-Donor-Bis-Acceptor Tribranched Organic Sensitizers for Dye-Sensitized Solar Cells." European Journal of Organic Chemistry 2011, no. 31 (2011): 6195–205. http://dx.doi.org/10.1002/ejoc.201100821.

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10

Leandri, Valentina, Riccardo Ruffo, Vanira Trifiletti, and Alessandro Abbotto. "Asymmetric Tribranched Dyes: An Intramolecular Cosensitization Approach for Dye-Sensitized Solar Cells." European Journal of Organic Chemistry 2013, no. 30 (2013): 6793–801. http://dx.doi.org/10.1002/ejoc.201300962.

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11

Hu, Jiangpu, Yang Li, Huaning Zhu та ін. "Photophysical Properties of Intramolecular Charge Transfer in a Tribranched Donor-π-Acceptor Chromophore". ChemPhysChem 16, № 11 (2015): 2357–65. http://dx.doi.org/10.1002/cphc.201500290.

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12

Lee, Geon Hyeong, and Young Sik Kim. "Effect of Tribranched Organic Dyes with Heteroleptic Dual Acceptor for Dye-Sensitized Solar Cells." Journal of Nanoscience and Nanotechnology 17, no. 11 (2017): 8383–88. http://dx.doi.org/10.1166/jnn.2017.15139.

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13

Li, Bo, Rui Tong, Rongyi Zhu, Fanshun Meng, He Tian, and Shixiong Qian. "The Ultrafast Dynamics and Nonlinear Optical Properties of Tribranched Styryl Derivatives Based on 1,3,5-Triazine." Journal of Physical Chemistry B 109, no. 21 (2005): 10705–10. http://dx.doi.org/10.1021/jp050368o.

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14

Jia, Mingli, Xiaonan Ma, Linyin Yan та ін. "Photophysical Properties of Intramolecular Charge Transfer in Two Newly Synthesized Tribranched Donor−π−Acceptor Chromophores". Journal of Physical Chemistry A 114, № 27 (2010): 7345–52. http://dx.doi.org/10.1021/jp1032355.

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15

Peyfoon, Elham, Benjamin Meyer, Paul G. Hitchen, et al. "The S-Layer Glycoprotein of the CrenarchaeoteSulfolobus acidocaldariusIs Glycosylated at Multiple Sites with Chitobiose-LinkedN-Glycans." Archaea 2010 (2010): 1–10. http://dx.doi.org/10.1155/2010/754101.

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Glycosylation of the S-layer of the crenarchaeaSulfolobus acidocaldariushas been investigated using glycoproteomic methodologies. The mature protein is predicted to contain 31 N-glycosylation consensus sites with approximately one third being found in the C-terminal domain spanning residuesL1004-Q1395. Since this domain is rich in Lys and Arg and therefore relatively tractable to glycoproteomic analysis, this study has focused on mapping its N-glycosylation. Our analysis identified nine of the 11 consensus sequence sites, and all were found to be glycosylated. This constitutes a remarkably hig

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16

Li, Bo, Rui Tong, Rongyi Zhu, Jianli Hua, He Tian, and Shixiong Qian. "The ultrafast dynamics and nonlinear optical properties of tribranched conjugated polymers with triphenylamine as the core." Journal of Luminescence 119-120 (July 2006): 116–21. http://dx.doi.org/10.1016/j.jlumin.2005.12.019.

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17

Santhosh, N. S., and G. Sundararajan. "Novel Linear and Tribranched Polymers with Redox-Active End Groups via W(CO)6-Initiated Metathesis Polymerization." Organic Letters 8, no. 4 (2006): 605–8. http://dx.doi.org/10.1021/ol052774w.

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18

Liu, Li, Wei Huang, Jieping Shi, Changgui Lü, Yiping Cui, and Guo-Yuan Lu. "Synthesis, Photophysical Properties of Tribranched Chromophores Based on 1,3,5-Triazine Core and Different Electro-donating End-groups." Chinese Journal of Chemistry 29, no. 10 (2011): 2129–33. http://dx.doi.org/10.1002/cjoc.201180369.

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19

Leandri, Valentina, Riccardo Ruffo, Vanira Trifiletti, and Alessandro Abbotto. "Asymmetric Tribranched Dyes: An Intramolecular Cosensitization Approach for Dye-Sensitized Solar Cells (Eur. J. Org. Chem. 30/2013)." European Journal of Organic Chemistry 2013, no. 30 (2013): n/a. http://dx.doi.org/10.1002/ejoc.201390085.

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20

Liu, Li, Zhiqiang Zhou, Jieping Shi, et al. "Photophysical and two-photon absorption properties of protonation-induced tribranched chromophore having 1,3,5-triazine core and pyrrole end-groups." Synthetic Metals 161, no. 9-10 (2011): 783–88. http://dx.doi.org/10.1016/j.synthmet.2011.01.030.

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21

Liu, Li, Wei Huang, Jieping Shi, Changgui Lue, Yiping Cui, and Guo-Yuan Lu. "ChemInform Abstract: Synthesis, Photophysical Properties of Tribranched Chromophores Based on 1,3,5-Triazine Core and Different Electro-Donating Eng-Groups." ChemInform 43, no. 8 (2012): no. http://dx.doi.org/10.1002/chin.201208203.

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22

Lee, Geon Hyeong, та Young Sik Kim. "Theoretical study of an asymmetric A-π-D-π-D-π-A′ tribranched organic sensitizer for dye-sensitized solar cells". Journal of the Korean Physical Society 69, № 3 (2016): 381–85. http://dx.doi.org/10.3938/jkps.69.381.

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23

Ikeda, Taichi. "Poly(ionic liquid)s Based on Copolymers of Poly(ethylene oxide) and Cationic Glycidyl Triazolyl Polymers with Tribranched Side Chains." ACS Macro Letters 10, no. 7 (2021): 831–36. http://dx.doi.org/10.1021/acsmacrolett.1c00253.

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24

Lee, Kyung-Hoon, Jun-Woo Lee, and Jung-Il Jin. "Liquid crystalline compounds having a tribranched structure: substituted malonic esters consisting of two Schiff's base units and a cholesteryloxyalkyl substituent." Liquid Crystals 28, no. 10 (2001): 1519–25. http://dx.doi.org/10.1080/02678290110071547.

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25

Fakis, M., I. Fitilis, S. Stefanatos, et al. "The photophysics and two-photon absorption of a series of quadrupolar and tribranched molecules: The role of the edge substituent." Dyes and Pigments 81, no. 1 (2009): 63–68. http://dx.doi.org/10.1016/j.dyepig.2008.08.014.

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26

Rao, Xianhua, Guodong Dang, Hongwei Zhou, et al. "Design and synthesis of a tribranched phenylethynyl-terminated aryl ether compound and its use as a reactive diluent for PETI-5." Journal of Polymer Science Part A: Polymer Chemistry 45, no. 21 (2007): 4844–54. http://dx.doi.org/10.1002/pola.22223.

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27

Lin, Jung-Fong, Ching-Fu Ho, and Steve K. Huang. "Studies on curing kinetics and total thermal degradation of the modified epoxy copolymer with penta-coordinated phosphate as a tribranched junction." Journal of Applied Polymer Science 77, no. 4 (2000): 719–32. http://dx.doi.org/10.1002/(sici)1097-4628(20000725)77:4<719::aid-app2>3.0.co;2-7.

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28

Xiang, Yong, Khanita Karaveg та Kelley W. Moremen. "Substrate recognition and catalysis by GH47 α-mannosidases involved in Asn-linked glycan maturation in the mammalian secretory pathway". Proceedings of the National Academy of Sciences 113, № 49 (2016): E7890—E7899. http://dx.doi.org/10.1073/pnas.1611213113.

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Maturation of Asn-linked oligosaccharides in the eukaryotic secretory pathway requires the trimming of nascent glycan chains to remove all glucose and several mannose residues before extension into complex-type structures on the cell surface and secreted glycoproteins. Multiple glycoside hydrolase family 47 (GH47) α-mannosidases, including endoplasmic reticulum (ER) α-mannosidase I (ERManI) and Golgi α-mannosidase IA (GMIA), are responsible for cleavage of terminal α1,2-linked mannose residues to produce uniquely trimmed oligomannose isomers that are necessary for ER glycoprotein quality contr

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29

BIAN, XUN, FU-MING SHI, and YAN-LIN CHANG. "Review of the genus Phlugiolopsis Zeuner, 1940 (Orthoptera: Tettigoniidae: Meconematinae) from China." Zootaxa 3281, no. 1 (2012): 1. http://dx.doi.org/10.11646/zootaxa.3281.1.1.

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This paper reviews the genus Phlugiolopsis Zeuner, 1940, and describes 5 new species from China, Phlugiolopsis pectinissp. nov., Phlugiolopsis tribranchis sp. nov., Phlugiolopsis digitusis sp. nov., Phlugiolopsis trullis sp. nov. andPhlugiolopsis adentis sp. nov. A key to the species and distributional data in China are given. The type specimens are deposited in the Museum of Hebei University.

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30

Gorochov, A. V. "New species of the genus Phlugiolopsis from its subgenus Omkoiana stat. nov. (Orthoptera: Tettigoniidae: Meconematinae)." Proceedings of the Zoological Institute RAS 324, no. 3 (2020): 346–52. http://dx.doi.org/10.31610/trudyzin/2020.324.3.346.

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The genus Phlugiolopsis Zeuner, 1940 is considered: its brief comparison with some similar genera is given, and its subgeneric composition is discussed. This genus is tentatively subdivided into two subgenera: Phlugiolopsis s. str. with three possible species; the subgenus Omkoiana Sänger et Helfert, 2002, stat. nov. with all the other species of this genus including three “subgenera” with unclear status (Longiloba Bian et Shi, 2018; Tribranchis Bian et Shi, 2018; Uncinata Bian et Shi, 2018). Two new species, Ph. (O.) trilobulata sp. nov. with three lobes on the male cercus and Ph. (O.) bilobu

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31

Hussein, Essam M., Nizar El Guesmi, and Saleh A. Ahmed. "Distinctive tunable photophysical properties of versatile environmentally-sensitive tribranched cyanopyridine fluorophores." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, November 2020, 119169. http://dx.doi.org/10.1016/j.saa.2020.119169.

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32

Liu, Li, Zhi Qiang Zhou, Jie Ping Shi, Chang Gui Lu, Yi Ping Cui, and Guo Yuan Lu. "Synthesis and properties of tribranched chromophores with triazine and fluorene units." Chinese Chemical Letters, July 2011. http://dx.doi.org/10.1016/j.cclet.2011.05.045.

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33

"2012 TriBranch Symposium." Lab Animal 41, no. 8 (2012): 215. http://dx.doi.org/10.1038/laban0812-215.

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34

"2013 Tribranch Symposium." Lab Animal 42, no. 8 (2013): 275. http://dx.doi.org/10.1038/laban.354.

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