Fan-bao Meng

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Name: Meng FanBao; 孟凡宝
Organization: Northeastern University
Department: Research Center for Molecular Science and Engineering
Title:

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Co-reporter:Dongyu Zhao, Lei Zhang, Lu Bai, Jingqi Luo, Xiaozhi He and Fan-bao Meng  
RSC Advances 2016 vol. 6(Issue 32) pp:26791-26799
Publication Date(Web):08 Mar 2016
DOI:10.1039/C5RA27247E
Novel chiral liquid-crystalline (LC) bromo-polysiloxanes (IP, IIP and IIIP) were graft copolymerized in a one-step hydrosilylation reaction by use of polymethylhydrogenosiloxane, cholest-5-en-3-ol(3β)-10-undecenoate and 4-bromobut-1-ene. A pyridyl-containing LC monomer cholesteryl isonicotinate (CIN) was synthesized and characterized. Some LC ionomers [IP–IIIP-Py][X] (X = Br) were synthesized by use of CIN and the bromo-polysiloxanes. Other LC ionomers [IP–IIIP-Py][X] (X = BF4, PF6, Tf2N) were prepared by metathesis of the pyridinium bromides. The chemical structure and liquid-crystalline properties were investigated by various experimental techniques. All the bromo-polysiloxanes display a smectic A (SA) mesophase when they are heated and cooled, while all these LC ionomers show a chiral smectic C (S*C) phase on heating, and exhibit SA and S*C phases on cooling. The LC ionomers show a narrower range of LC temperature than the corresponding bromo-polysiloxanes. For the LC ionomers bearing homologous pyridinium cations and different anions, the glass transition temperature, mesophase–isotropic phase transition temperature and LC temperature range tend to reduce, and the spontaneous polarization value increases slightly in the sequence of Br−, BF4−, PF6−, and Tf2N−. Rearrangement of smectic layers due to electrostatic attraction and ion aggregation of cholesteryl pyridinium salt mesogens lead to the formation of the S*C phase for these LC ionomers.
Co-reporter:Jingqi Luo;Jinmin Lu;Dongyu Zhao;Xinyu Du;Xiaozhi He ;Fanbao Meng
Polymers for Advanced Technologies 2016 Volume 27( Issue 3) pp:290-302
Publication Date(Web):
DOI:10.1002/pat.3634

A series of polymerized ionic liquid crystals (PILCs) bearing fluorinated cholesteryl mesogens were synthesized in this work, which include polymerized imidazolium bromides (PIBs) and polymerized imidazolium hexafluorophosphates (PIHs). The PIBs were synthesized using alkyl bromine-containing polysiloxanes and 1-butyl-1H-imidazole, and the PIHs were synthesized by anion metathesis reaction using the corresponding PIBs and KPF6. The chemical structures, liquid crystalline (LC) properties, and electrorheological (ER) effect of these PILCs were characterized by use of various experimental techniques. All the PILCs showed smectic A mesophase on heating and cooling cycles. The smectic layer structure of these PILCs are originated from the rigid fluorinated cholesteryl mesogens and the flexible moieties in the LC phase, but the ion pairs (imidazolium cations–PF6, Im+–PF6; or imidazolium cations–Br, Im+–Br) can disperse in the polysiloxane matrix and expand the d-spacing in the smectic layers. The PIHs show lower Tg and Ti than the corresponding precursor PIBs, which is due to the larger ion volume of Im+–PF6 for PIHs than that of Im+–Br for PIBs. A series of 40 V% ER fluids were prepared by mixing the PILCs with polydimethylsiloxane (PDMS), and the ER behaviors were studied. All the PILC/PDMS fluids showed ER effect, and the PIH/PDMS fluids show a little greater ER effect than the PIB/PDMS fluids. The PILC droplets in the ER fluids become deformed owing to both the orientation of fluorinated cholesteryl mesogens and the suppression of ionic migration when a DC electric field was applied, resulting in the occurrence of ER effect. Copyright © 2015 John Wiley & Sons, Ltd.

Co-reporter:Shuang Ma;Xin Li;Lu Bai;Xin Lan;Naiyu Zhou;Fanbao Meng
Colloid and Polymer Science 2015 Volume 293( Issue 8) pp:2257-2268
Publication Date(Web):2015 August
DOI:10.1007/s00396-015-3617-5
A series of polymerized ionic liquid crystals (PILCs) with different anions were synthesized and characterized, including bromides (PIBs), tetrafluoroborates (PITs), hexafluorophosphates (PIHs), trifluoromethanesulfonates (PITFs), and bis(trifluoromethylsulfonyl)imides (PIBTs). The PIBs show both smectic A (SmA) phase and chiral nematic (N*) mesophases on heating and cooling cycles, but other PILCs exhibit only chiral nematic mesophase. The glass transition temperature (Tg) of the PIBs, PIHs, PITs, PITFs, and PIBTs decreases successively, but the isotropic temperature (Ti) shows no big change. All these PILCs display ionic conductivity in mesophase. The PITs present a little higher ionic conductivity than other PILCs indicating that the ionic conductivities of these PILCs depend on the nature of the anions. The molecular packing of these PILCs is distinct from each other due to different anions. The bromides (PIBs) should form intimate ion pairs, but other PILCs should form ion clusters rather than ion pairs due to large size of anions.
Co-reporter:Fanbao Meng;Lu Bai;Shuang Ma;Xin Lan;Xin Li
Colloid and Polymer Science 2014 Volume 292( Issue 7) pp:1511-1519
Publication Date(Web):2014 July
DOI:10.1007/s00396-014-3204-1
A series of chiral fluorinated liquid-crystalline elastomers (LCEs) IP-VIP are prepared by 4-cyano-3-fluorophenyl 4′-(undec-10-enoyloxy)biphenyl-4-carboxylate, isosorbide bis(4-allyloxybenzoate) and 2,4,6,8-tetramethylcyclotetrasiloxane via Pt-catalyzed hydrosilylation. The chiral crosslinking moieties increase from IP to IVP. The elastomers IP, IIP, and IIIP containing low content of chiral crosslinking moieties display SC* liquid-crystalline phase, but IVP, VP, and VIP do not show SC* phase except for N* mesophase. The mesophase is testified according to typical diffractogram measured by X-ray diffraction (XRD) analysis. The layer spacings of the LCEs decrease from IP (d-spacing of 34.2 Å) to VIP (d-spacing of 31.6 Å) with increase of chiral crosslinking groups in the polymers systems. Moreover, the optical properties are performed by ultraviolet–visible–near-infrared spectrophotometry. VP and VIP containing the most chiral crosslinking moieties display maximum reflection in near infrared spectra in the measurement of optical properties, while IP, IIP, IIIP, and IVP do not show obvious maximum reflection. It is interesting that a specific reflection of circularly polarized light appears along with a changing mesophase due to high enough concentration of chiral crosslinking dopants for VP and VIP. All these results suggest that the chiral crosslinking moieties exert influence on the structures of these kinds of LCEs.
Co-reporter:Xin Lan, Lu Bai, Xin Li, Shuang Ma, Xiaozhi He, Fanbao Meng
Journal of Molecular Structure 2014 1075() pp: 515-524
Publication Date(Web):5 October 2014
DOI:10.1016/j.molstruc.2014.07.026
Co-reporter:Fan-bao Meng, Chang Du, Nai-yu Zhou, Xiao-Zhi He, Hai-bin Chen
European Polymer Journal 2013 Volume 49(Issue 10) pp:3392-3401
Publication Date(Web):October 2013
DOI:10.1016/j.eurpolymj.2013.07.020
•Chiral liquid-crystalline elastomers were synthesized by hydrosilylation reaction.•The fluorinated chiral elastomers show chiral smectic C mesophase.•The fluorinated chiral elastomers display spontaneous polarization.•The glass transition temperature increases with increase of chiral crosslinking mesogens.Fluorinated chiral liquid-crystalline elastomers (LCEs) were graft copolymerized by a one-step hydrosilylation reaction with polymethylhydrogenosiloxane, a fluorinated LC monomer 4-(2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoyloxy)phenyl 4-(undec-10-enoyloxy)benzoate (PPUB) and a chiral crosslinking LC monomer (3R,3aR,6S,6aR)-6-(undec-10-enoyloxy)hexahydrofuro[3,2-b]furan-3-yl 4′-(4-(allyloxy)benzoyloxy)biphenyl-4-carboxylate (UHAB). The chemical structure, liquid-crystalline behavior and polarization property were characterized by use of various experimental techniques. The effective crosslink density of the LCEs was characterized by swelling experiments. The thermal analysis results showed that the temperatures at which 5% weight loss occurred were greater than 250 °C for all the LCEs, and the residue weight nearby 600 °C increase with increasing chiral crosslinking components in the polymer systems. All the samples showed chiral smectic C mesophase when they were heated. The glass transition temperature and mesophase-isotropic phase transition temperature of fluorinated elastomers increased slightly with increase of chiral crosslinking mesogens in the polymer systems, but the enthalpy changes of mesophase-isotropic phase transition decreased slightly. In XRD curves, all the samples exhibited strong sharp reflections at small angles suggesting smectic layered packing arrangement. These fluorinated chiral LCEs showed 0.1–0.2 μC/cm2 of spontaneous polarization with increasing chiral crosslinking component.Graphical abstract
Co-reporter:Fan-Bao Meng;Nai-Yu Zhou;Chang Du;Hong-Mei Gao ;Xiao-Zhi He
Journal of Applied Polymer Science 2013 Volume 130( Issue 5) pp:3395-3403
Publication Date(Web):
DOI:10.1002/app.39593

ABSTRACT

A series of main-chain liquid-crystalline polymers (LCPs) with pendant sulfonic acid groups have been synthesized by use of biphenyl-4,4′-diol, 6,7-dihydroxynaphthalene-2-sulfonic acid, and bis(4-(chlorocarbonyl)phenyl) decanedioate in a one-step esterification reaction. Emeraldine base form of polyaniline (PAN) is doped by the synthesized sulfonic acid-containing LCPs to obtain PAN–LCP ionomers. A series of electrorheological (ER) fluids are prepared using the synthesized PAN–LCP ionomers and silicone oil. The chemical structure, liquid-crystalline behavior, dielectric property of LCPs, and PAN–LCP ionomers, and ER effect of the ER fluids are characterized by use of various experimental techniques. The synthesized sulfonic acid-containing LCPs and PAN–LCP ionomers display nematic mesophase. The PAN–LCP ionomers show a slight elevation of glass transition temperatures and decrease of enthalpy changes of nematic–isotropic phase transition compared with corresponding sulfonic acid-containing LCPs. The relative permittivity of the PAN–LCP ionomers is much higher than that of the corresponding sulfonic acid-containing LCPs. The ER effect of the PAN–LCP ionomer dispersions is better than PAN dispersions, suggesting a synergistic reaction should be occurred among liquid crystalline component, and PAN part under electric fields. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3395–3403, 2013

Co-reporter:Fan-Bao Meng;Xiao-Zhi He;Xiao-Dong Zhang;Yue Ma
Colloid and Polymer Science 2011 Volume 289( Issue 8) pp:955-965
Publication Date(Web):2011 June
DOI:10.1007/s00396-011-2417-9
A novel perfluorinated liquid crystal 4′-(2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoyloxy)biphenyl-4-yl undec-10-enoate (PFOBU) was synthesized, which exhibited smectic C phase. Several liquid crystalline polymers (PI–PVI) were synthesized by use of poly(methylhydrogeno)siloxane, PFOBU, and cholesteryl 3-(4-allyloxy-phenyl)-acryloate. The chemical structures and liquid crystalline (LC) properties of the monomers and polymers, and some ferroelectric properties of the chiral smectic C (SC*) phase were characterized by use of various experimental techniques. The effect of perfluorocarbon chains on phase behaviors of the fluorinated LC polysiloxanes was studied as well. PI and PII showed single chiral nematic (N*) mesophase when they were heated and cooled, but PIII, PIV, PV, and PVI containing more perfluorocarbon chain units exhibited SC* phase besides N* mesophase. Introduction of perfluorocarbon chain containing mesogens to the chiral cholesteryl-containing polymer systems resulted in a SC* mesophases, indicating that the fluorophobic effect could lead to microphase segregation and modifications of smectic mesophases from the chiral nematic phase.
Co-reporter:Fan-Bao Meng, Xiao-Dong Zhang, Xiao-Zhi He, He Lu, Yue Ma, Hui-Li Han, Bao-Yan Zhang
Polymer 2011 Volume 52(Issue 22) pp:5075-5084
Publication Date(Web):13 October 2011
DOI:10.1016/j.polymer.2011.09.002
Several novel chiral side-chain liquid crystalline (LC) polysiloxane resins containing epoxy groups and mesogenic components have been graft copolymerized by a one-step hydrosilylation reaction with poly(methylhydrogeno)siloxane, an epoxy monomer 2-(allyloxymethyl)oxirane, and chiral fluorinated liquid-crystalline monomers 4′-(4-(allyloxy)benzoyloxy)biphenyl-4-yl 6-(perfluorooctanoyloxy)hexahydrofuro[3,2-b]furan-3-yl adipate and 4′-(4-(undec-10-enoyloxy)benzoyloxy)biphenyl-4-yl 6-(perfluorooctanoyloxy)hexahydrofuro[3,2-b]furan-3-yl adipate. The synthesized epoxy resins are cured using 4,4′-diaminodiphenyl-methane in mesophase state under a magnetic field to obtain crosslinked oriented elastomers. The chemical structures, LC properties and surface morphology of the monomers, the resins and the liquid crystalline elastomers (LCEs) are characterized by use of various experimental techniques such as FTIR, 1H NMR, EA, TGA, DSC, POM, and X-ray measurements. The mesomorphic properties of the synthesized resins and corresponding oriented elastomers are influenced by the terminal perfluorocarbon chains components effectively. The resins show chiral nematic and chiral smectic C phases (Sc*), and Sc* are frozen in their corresponding oriented elastomers. The LC phases are verified by X-ray measurements, and the orientational order parameters of the oriented LCEs are calculated as well.
Cholest-5-en-3-ol (3β)-, 3-[2-fluoro-4-(2-propen-1-yloxy)benzoate]