Výsledky vyhledávání - "Elsegood, Mark RJ"

Allosteric binding properties of a 1,3-alternate thiacalix[4]arene-based receptor having phenylthiourea and 2-pyridylmethyl moieties on opposite faces

Autor: Rahman, Shofiur, Tomiyasu, Hirotsugu, Wang, Chuan-Zeng, Georghiou, Paris E, Alodhayb, Abdullah, Carpenter-Warren, Cameron L, Elsegood, Mark RJ, Teat, Simon J, Redshaw, Carl, Yamato, Takehiko

Publikováno v: New Journal of Chemistry, vol 45, iss 41

The synthesis of three new heteroditopic receptors (5a-c) which are based on thiacalix[4]arenes in the 1,3-alternate conformation is reported herein. These new receptors each have two thiourea moieties linking phenyl groups, two of which are substitu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::aea4ce71b75380d355db48b982a2b60e
https://escholarship.org/uc/item/4p34g3dx

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Pyrene-fused hexaarylbenzene luminogens: Synthesis, characterization, and aggregation-induced emission enhancement

Autor: Wang, Chuan-Zeng, Yu, Ze-Dong, Zhao, Wen-Xuan, Yang, Kai, Noda, Yuki, Zhao, Yi, Feng, Xing, Elsegood, Mark RJ, Teat, Simon J, Redshaw, Carl, Yamato, Takehiko

Six novel pyrene-fused hexaarylbenzene derivatives (3a-f) were designed, synthesized, and characterized, which exhibited aggregation-induced emission enhancement (AIEE) in the aggregated state by means of THF/H2O mixtures. Techniques such as theoreti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::2c46e298d61900415313af5bb1c265e7
https://escholarship.org/uc/item/5js39905

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Effect of Alkyl Chain Length and Linker Atom on the Crystal Packing in 6,12-Dialkoxy- and 6,12-Dialkylsulfanyl-Benzo[1,2‑b:4,5‑b′]bis[b]benzothiophenes

Autor: Riaz, Shahzad, Edgar, Mark, Elsegood, Mark RJ, Horsburgh, Lynne, Teat, Simon J, Warwick, Thomas G, Weaver, George W

Publikováno v: Crystal Growth & Design, vol 19, iss 9

The effect of varying the chain length on the solid state conformation and packing of 6,12-dialkoxy- and 6,12-dialkylsulfanyl-benzo[1,2-b:4,5-b′]bis[b]benzothiophenes has been studied. The compounds were prepared by SNAr reaction of 6,12-difluorben

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::9790e475b201b4ec604bc1863f58e738
https://escholarship.org/uc/item/1hw5d8cw

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Pyrene‐Fused Pyrazaacenes with Eight Rectilinearly Arranged Aromatic Rings

Autor: Wang, Chuan‐Zeng, Feng, Xing, Elsegood, Mark RJ, Warwick, Thomas G, Teat, Simon J, Redshaw, Carl, Bi, Yu‐Sui, Yamato, Takehiko

Publikováno v: Asian Journal of Organic Chemistry, vol 8, iss 1

A series of pyrene-fused azaacene-type conjugated molecules containing two pyrazine units and up to eight rectilinearly arranged aromatic rings were prepared by condensation coupling reactions in moderate yields. The geometries and electronic structu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::71ec226e6e68b5c879543590ad07780d
https://escholarship.org/uc/item/3mx164sd

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Thiacalix[4]arene Derivatives Bearing Imidazole Units: A Ditopic Hard/Soft Receptor for Na+ and K+/Ag+ with an Allosteric Effect and a Reusable Extractant for Dichromate Anions

Autor: Zhao, Jiang‐Lin, Wu, Chong, Zeng, Xi, Rahman, Shofiur, Georghiou, Paris E, Elsegood, Mark RJ, Warwick, Thomas G, Redshaw, Carl, Teat, Simon J, Yamato, Takehiko

Publikováno v: ChemistrySelect, vol 1, iss 8

Two novel receptors 5,11,17,23-tetra-tert-butyl-25,27-bis[(ethoxycarbonyl)methoxy]-26,28-bis-[1-methyl-(imidazole)meth-oxy]-2,8,14,20-tetra-thiacalix[4]arene (L1) and 5,11,17,23-tetra-tert-butyl-25,27-bis-[(benzyl)methoxy]-26,28-bis-[1-methyl-(imidaz

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2421c13bb567f889382bdb54782382e6
https://escholarship.org/uc/item/9zd802p9

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Akademický článek

Sulfimidation of thio-ether crown systems: the X-ray crystal structure of the {[9-ane]S[sub 2] S(NH[sub 2] )}[sup +] , {[9-ane]SS(NH[sub 2] )S(NH[sub 2] )}[sup 2+] , and {[9-ane]S(NH[sub 2] )S[sub 2] (µ-N)}[sup 2+] cations.

Autor: Gilby, Liam M, Holmes, Kathryn E, Kelly, Paul F, Elsegood, Mark RJ

Publikováno v: Canadian Journal of Chemistry; Nov2002, Vol. 80 Issue 11, p1410-1414, 5p

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