Guan-Yeow Yeap
Universiti Sains Malaysia
182 Papers
1.2K Citations
Guan-Yeow Yeap is an academic researcher from Universiti Sains Malaysia. The author has contributed to research in topics: Liquid crystal & Schiff base. The author has an hindex of 23, co-authored 170 publications. Previous affiliations of Guan-Yeow Yeap include Universiti Tunku Abdul Rahman.
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Papers
Cholesteryl-based liquid crystal dimers containing a sulfur–sulfur link in the flexible spacer
Huey-Charn Lee,Zhibao Lu,Peter A. Henderson,Wan Ahmad Kamil Mahmood,Guan-Yeow Yeap,Corrie T. Imrie +5 more
TL;DR: In this paper, seven members of the bis(ω-(cholesteryloxycarbonyl)alkyl) disulfides, which contain a sulfur−sulfur link in the flexible spacer have been synthesized and their liquid crystal properties characterised.
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Non-symmetric liquid crystal dimers containing an isoflavone moiety
TL;DR: The first series of liquid crystal dimers to contain an isoflavone-based moiety has been prepared, the α-(4'-methoxy-3-phenyl-4H-1-benzopyran-4-one-7-oxy)-ω-(4-methioxazobenzene-4'-oxy)alkanes as discussed by the authors.
128
Why do non-symmetric dimers intercalate? The synthesis and characterisation of the α-(4-benzylidene-substituted-aniline-4′-oxy)-ω-(2-methylbutyl-4′-(4″-phenyl)benzoateoxy)alkanes
Guan-Yeow Yeap,Tiang-Chuan Hng,Sue-Yi Yeap,Ewa Gorecka,Masato M. Ito,Koichi Ueno,Masaki Okamoto,Wan Ahmad Kamil Mahmood,Corrie T. Imrie +8 more
TL;DR: In this article, 10 new non-symmetric liquid crystal dimers belonging to the family of compounds α-(4-benzylidene-substituted-aniline-4′-oxy)-ω-(2-methylbutyl)-4′-(4″-phenyl)benzoateoxy)-alkanes have been synthesised and their transitional properties characterised.
120
Non-symmetric dimers: effects of varying the mesogenic linking unit and terminal substituent
TL;DR: In this article, six new non-symmetric dimers belonging to the family of compounds the (R,S)-(benzylidene-4-substituted-aniline)-2ʺ-methylbutyl-4ʹʹ-phenyloxy) benzoate-oxy) hexanoates have been prepared and their thermal behaviour characterised.
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Synthesis, physical and mesomorphic properties of Schiff's base esters containing ortho‐, meta‐ and para‐substituents in benzylidene‐4′‐alkanoyloxyanilines
Guan-Yeow Yeap,Sie-Tiong Ha,Phaik-Leng Lim,Peng-Lim Boey,Masato M. Ito,Shigeki Sanehisa,Yamashita Youhei +6 more
TL;DR: In this paper, the effect of lateral methoxy and polar hydroxy groups on the mesomorphism of Schiff's base esters was studied, based on thermal properties and textural analysis, which indicated that compounds with the larger number of carbons in the alkyl chain prefer smectic phase formation and possess higher transition temperatures and molecular polarizability along the long axis.
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