Výsledky vyhledávání - "Hsin Chieh Tiao"

Effect of hydroxyl density on condensation behaviors of self-assembled monolayers and performance of pentacene-base organic thin-film transistors

Autor: Yao-Jen Lee, Shu-Hsien Lee, Ming-Yu Kuo, Hsin-Chieh Tiao, Ching-Hsiu Li, Yi-Shan Liu

Publikováno v: Organic Electronics. 13:1004-1011

A series of self-assembled monolayers (SAMs), comprising octadecyltrichlorosilane (ODTS), dodecyltrichlorosilane (DDTS), and hexamethyldisilazane (HMDS), were prepared to examine the effects of phase states and condensation behaviors of SAMs on the m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5f57bd364f69deac6cd0b0e89d85eddc
https://doi.org/10.1016/j.orgel.2012.03.004

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Nickel-Catalyzed, Cascade Cycloadditions of 1-Ethynyl-8-halonaphthalenes with Nitriles: Synthesis, Structure, and Physical Properties of New Pyrroloarenes

Autor: Hsin Chieh Tiao, Tsun Cheng Wu, Ming-Yu Kuo, Yao‐Ting Wu, Chia Cheng Tai

Publikováno v: Chemistry - A European Journal. 17:1930-1935

The reaction of 1-ethynyl-8-halonaphthalenes 1 with nitriles in the presence of the catalytic system [NiBr(2)(dppe)]/Zn (dppe=1,2-bis(diphenylphosphino)ethane) is found to produce unusual pyrroloarenes 2. The carbon-nitrogen triple bond in nitrile is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eab36c8ccd4a0145bca80e4650a8c388
https://doi.org/10.1002/chem.201002905

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ChemInform Abstract: Palladium-Catalyzed Cycloisomerizations of Diarylacetylenes: Synthesis, Structures, and Physical Properties of Highly Substituted Naphthalenes and 8,8a-Dihydrocyclopenta[a]indenes

Autor: Cheng-Hao Huang, Ching-Hsiu Li, Hsin-Chieh Tiao, Ming‐Yu Kuo, Chia-Chun Liu, Tsun‐Cheng Wu, Yao‐Ting Wu, Chia-Cheng Tai, Yu‐Ting Chang

Publikováno v: ChemInform. 42

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::062fa265773e740da0be71c8f943466b
https://doi.org/10.1002/chin.201141084

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Palladium-catalyzed cycloisomerizations of diarylacetylenes: synthesis, structures, and physical properties of highly substituted naphthalenes and 8,8 a-dihydrocyclopenta[a]indenes

Autor: Tsun Cheng Wu, Yu‐Ting Chang, Hsin Chieh Tiao, Ming-Yu Kuo, Cheng Hao Huang, Yao‐Ting Wu, Chia Chun Liu, Chia Cheng Tai, Ching Hsiu Li

Publikováno v: Chemistry (Weinheim an der Bergstrasse, Germany). 17(26)

Depending on the electronic properties of their substituents, the major products generated by palladium-catalyzed cycloisomerizations of diarylalkynes are either highly substituted 8,8a-dihydrocyclopenta[a]indenes 3 or naphthalenes 4. The structures

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f9c5093b27eec23cfe750154f3e298a
https://pubmed.ncbi.nlm.nih.gov/21567502

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