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Redox active dendronized polystyrenes equipped with peripheral triarylamines.

Beilstein journal of organic chemistry

Nokami T, Musya N, Morofuji T, Takeda K, Takumi M, Shimizu A, Yoshida J.
PMID: 25670978
Beilstein J Org Chem. 2014 Dec 22;10:3097-103. doi: 10.3762/bjoc.10.326. eCollection 2014.

Dendronized polystyrene having peripheral bromo groups was prepared from the dendronization of unfunctionalized polystyrene with dendritic diarylcarbenium ions bearing peripheral bromo groups using the "cation pool" method. The palladium-catalyzed amination of the peripheral bromo groups with diarylamine gave dendronized...

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Nokami T, Musya N, Morofuji T, et al. Redox active dendronized polystyrenes equipped with peripheral triarylamines. Beilstein J Org Chem. 2014;10:3097-103doi: 10.3762/bjoc.10.326.
Nokami, T., Musya, N., Morofuji, T., Takeda, K., Takumi, M., Shimizu, A., & Yoshida, J. (2014). Redox active dendronized polystyrenes equipped with peripheral triarylamines. Beilstein journal of organic chemistry, 103097-103. https://doi.org/10.3762/bjoc.10.326
Nokami, Toshiki, et al. "Redox active dendronized polystyrenes equipped with peripheral triarylamines." Beilstein journal of organic chemistry vol. 10 (2014): 3097-103. doi: https://doi.org/10.3762/bjoc.10.326
Nokami T, Musya N, Morofuji T, Takeda K, Takumi M, Shimizu A, Yoshida J. Redox active dendronized polystyrenes equipped with peripheral triarylamines. Beilstein J Org Chem. 2014 Dec 22;10:3097-103. doi: 10.3762/bjoc.10.326. eCollection 2014. PMID: 25670978; PMCID: PMC4311719.
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Surface segregation driven by molecular architecture asymmetry in polymer blends.

Physical review letters

Lee JS, Lee NH, Peri S, Foster MD, Majkrzak CF, Hu R, Wu DT.
PMID: 25494077
Phys Rev Lett. 2014 Nov 28;113(22):225702. doi: 10.1103/PhysRevLett.113.225702. Epub 2014 Nov 26.

The contributions of chain ends and branch points to surface segregation of long-branched chains in blends with linear chains have been studied using neutron reflectometry and surface-enhanced Raman spectroscopy for a series of novel, well-defined polystyrenes. A linear response...

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Lee JS, Lee NH, Peri S, et al. Surface segregation driven by molecular architecture asymmetry in polymer blends. Phys Rev Lett. 2014;113(22):225702doi: 10.1103/PhysRevLett.113.225702.
Lee, J. S., Lee, N. H., Peri, S., Foster, M. D., Majkrzak, C. F., Hu, R., & Wu, D. T. (2014). Surface segregation driven by molecular architecture asymmetry in polymer blends. Physical review letters, 113(22), 225702. https://doi.org/10.1103/PhysRevLett.113.225702
Lee, Jae Sik, et al. "Surface segregation driven by molecular architecture asymmetry in polymer blends." Physical review letters vol. 113,22 (2014): 225702. doi: https://doi.org/10.1103/PhysRevLett.113.225702
Lee JS, Lee NH, Peri S, Foster MD, Majkrzak CF, Hu R, Wu DT. Surface segregation driven by molecular architecture asymmetry in polymer blends. Phys Rev Lett. 2014 Nov 28;113(22):225702. doi: 10.1103/PhysRevLett.113.225702. Epub 2014 Nov 26. PMID: 25494077.
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Structure and luminescent property of complexes of aryl carboxylic acid-functionalized polystyrene with Eu(III) and Tb(III) ions.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Gao B, Shi N, Qiao Z.
PMID: 26086996
Spectrochim Acta A Mol Biomol Spectrosc. 2015 Nov 05;150:565-74. doi: 10.1016/j.saa.2015.05.078. Epub 2015 May 30.

Via polymer reactions, naphthoic acid (NA) and benzoic acid (BA) were bonded onto the side chains of polystyrene (PS), respectively, and two aryl carboxylic acid-functionalized polystyrenes, PSNA and PSBA, were obtained. Using PSNA and PSBA as macromolecule ligands and...

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Gao B, Shi N, Qiao Z. Structure and luminescent property of complexes of aryl carboxylic acid-functionalized polystyrene with Eu(III) and Tb(III) ions. Spectrochim Acta A Mol Biomol Spectrosc. 2015;150:565-74doi: 10.1016/j.saa.2015.05.078.
Gao, B., Shi, N., & Qiao, Z. (2015). Structure and luminescent property of complexes of aryl carboxylic acid-functionalized polystyrene with Eu(III) and Tb(III) ions. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 150565-74. https://doi.org/10.1016/j.saa.2015.05.078
Gao, Baojiao, et al. "Structure and luminescent property of complexes of aryl carboxylic acid-functionalized polystyrene with Eu(III) and Tb(III) ions." Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy vol. 150 (2015): 565-74. doi: https://doi.org/10.1016/j.saa.2015.05.078
Gao B, Shi N, Qiao Z. Structure and luminescent property of complexes of aryl carboxylic acid-functionalized polystyrene with Eu(III) and Tb(III) ions. Spectrochim Acta A Mol Biomol Spectrosc. 2015 Nov 05;150:565-74. doi: 10.1016/j.saa.2015.05.078. Epub 2015 May 30. PMID: 26086996.
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Bis(phenolate)amine-supported lanthanide borohydride complexes for styrene and trans-1,4-isoprene (co-)polymerisations.

Dalton transactions (Cambridge, England : 2003)

Bonnet F, Dyer HE, El Kinani Y, Dietz C, Roussel P, Bria M, Visseaux M, Zinck P, Mountford P.
PMID: 25997125
Dalton Trans. 2015 Jul 21;44(27):12312-25. doi: 10.1039/c5dt00252d.

New bis(phenolate)amine-supported neodymium borohydride complexes and their previously reported samarium analogues were tested as catalysts for the polymerisation of styrene and isoprene. Reaction of Na2O2N(L) (L = py, OMe, NMe2) with Nd(BH4)3(THF)3 afforded the borohydride complexes Nd(O2N(L))(BH4)(THF) (L =...

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Bonnet F, Dyer HE, El Kinani Y, et al. Bis(phenolate)amine-supported lanthanide borohydride complexes for styrene and trans-1,4-isoprene (co-)polymerisations. Dalton Trans. 2015;44(27):12312-25doi: 10.1039/c5dt00252d.
Bonnet, F., Dyer, H. E., El Kinani, Y., Dietz, C., Roussel, P., Bria, M., Visseaux, M., Zinck, P., & Mountford, P. (2015). Bis(phenolate)amine-supported lanthanide borohydride complexes for styrene and trans-1,4-isoprene (co-)polymerisations. Dalton transactions (Cambridge, England : 2003), 44(27), 12312-25. https://doi.org/10.1039/c5dt00252d
Bonnet, Fanny, et al. "Bis(phenolate)amine-supported lanthanide borohydride complexes for styrene and trans-1,4-isoprene (co-)polymerisations." Dalton transactions (Cambridge, England : 2003) vol. 44,27 (2015): 12312-25. doi: https://doi.org/10.1039/c5dt00252d
Bonnet F, Dyer HE, El Kinani Y, Dietz C, Roussel P, Bria M, Visseaux M, Zinck P, Mountford P. Bis(phenolate)amine-supported lanthanide borohydride complexes for styrene and trans-1,4-isoprene (co-)polymerisations. Dalton Trans. 2015 Jul 21;44(27):12312-25. doi: 10.1039/c5dt00252d. PMID: 25997125.
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Structure, Optical Absorption, and Performance of Organic Solar Cells Improved by Gold Nanoparticles in Buffer Layers.

ACS applied materials & interfaces

Yang Y, Feng S, Li M, Wu Z, Fang X, Wang F, Geng D, Yang T, Li X, Sun B, Gao X.
PMID: 26477556
ACS Appl Mater Interfaces. 2015 Nov 11;7(44):24430-7. doi: 10.1021/acsami.5b07983. Epub 2015 Oct 27.

11-Mercaptoundecanoic acid (MUA)-stabilized gold nanoparticles (AuNPs) embedded in copper phthalocyanine (CuPc) were used as a buffer layer between a poly(3-hexyl-thiophene) (P3HT)/[6,6]-phenyl C61-butyric acid methyl ester (PCBM) bulk heterojunction and anodic indium-tin oxide (ITO) substrate. As systematic synchrotron-based grazing incidence...

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Yang Y, Feng S, Li M, et al. Structure, Optical Absorption, and Performance of Organic Solar Cells Improved by Gold Nanoparticles in Buffer Layers. ACS Appl Mater Interfaces. 2015;7(44):24430-7doi: 10.1021/acsami.5b07983.
Yang, Y., Feng, S., Li, M., Wu, Z., Fang, X., Wang, F., Geng, D., Yang, T., Li, X., Sun, B., & Gao, X. (2015). Structure, Optical Absorption, and Performance of Organic Solar Cells Improved by Gold Nanoparticles in Buffer Layers. ACS applied materials & interfaces, 7(44), 24430-7. https://doi.org/10.1021/acsami.5b07983
Yang, Yingguo, et al. "Structure, Optical Absorption, and Performance of Organic Solar Cells Improved by Gold Nanoparticles in Buffer Layers." ACS applied materials & interfaces vol. 7,44 (2015): 24430-7. doi: https://doi.org/10.1021/acsami.5b07983
Yang Y, Feng S, Li M, Wu Z, Fang X, Wang F, Geng D, Yang T, Li X, Sun B, Gao X. Structure, Optical Absorption, and Performance of Organic Solar Cells Improved by Gold Nanoparticles in Buffer Layers. ACS Appl Mater Interfaces. 2015 Nov 11;7(44):24430-7. doi: 10.1021/acsami.5b07983. Epub 2015 Oct 27. PMID: 26477556.
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Omnidirectional Harvesting of Weak Light Using a Graphene Quantum Dot-Modified Organic/Silicon Hybrid Device.

ACS nano

Tsai ML, Tsai DS, Tang L, Chen LJ, Lau SP, He JH.
PMID: 28430415
ACS Nano. 2017 May 23;11(5):4564-4570. doi: 10.1021/acsnano.6b08567. Epub 2017 Apr 27.

Despite great improvements in traditional inorganic photodetectors and photovoltaics, more progress is needed in the detection/collection of light at low-level conditions. Traditional photodetectors tend to suffer from high noise when operated at room temperature; therefore, these devices require additional...

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Tsai ML, Tsai DS, Tang L, et al. Omnidirectional Harvesting of Weak Light Using a Graphene Quantum Dot-Modified Organic/Silicon Hybrid Device. ACS Nano. 2017;11(5):4564-4570doi: 10.1021/acsnano.6b08567.
Tsai, M. L., Tsai, D. S., Tang, L., Chen, L. J., Lau, S. P., & He, J. H. (2017). Omnidirectional Harvesting of Weak Light Using a Graphene Quantum Dot-Modified Organic/Silicon Hybrid Device. ACS nano, 11(5), 4564-4570. https://doi.org/10.1021/acsnano.6b08567
Tsai, Meng-Lin, et al. "Omnidirectional Harvesting of Weak Light Using a Graphene Quantum Dot-Modified Organic/Silicon Hybrid Device." ACS nano vol. 11,5 (2017): 4564-4570. doi: https://doi.org/10.1021/acsnano.6b08567
Tsai ML, Tsai DS, Tang L, Chen LJ, Lau SP, He JH. Omnidirectional Harvesting of Weak Light Using a Graphene Quantum Dot-Modified Organic/Silicon Hybrid Device. ACS Nano. 2017 May 23;11(5):4564-4570. doi: 10.1021/acsnano.6b08567. Epub 2017 Apr 27. PMID: 28430415.
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A Novel and Facile One-Pot Solvothermal Synthesis of PEDOT-PSS/Ni-Mn-Co-O Hybrid as an Advanced Supercapacitor Electrode Material.

ACS applied materials & interfaces

Yin C, Yang C, Jiang M, Deng C, Yang L, Li J, Qian D.
PMID: 26794146
ACS Appl Mater Interfaces. 2016 Feb 03;8(4):2741-52. doi: 10.1021/acsami.5b11022. Epub 2016 Jan 21.

In this work, a novel and facile one-pot method has been developed for the synthesis of a hybrid consisting of Ni-Mn-Co ternary oxide and poly(3,4-ethylenedioxythiophene)-polystyrenesulfonate (PEDOT-PSS/NMCO) with a hierarchical three-dimensional net structure via a solvothermal-coprecipitation coupled with oxidative polymerization...

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Yin C, Yang C, Jiang M, et al. A Novel and Facile One-Pot Solvothermal Synthesis of PEDOT-PSS/Ni-Mn-Co-O Hybrid as an Advanced Supercapacitor Electrode Material. ACS Appl Mater Interfaces. 2016;8(4):2741-52doi: 10.1021/acsami.5b11022.
Yin, C., Yang, C., Jiang, M., Deng, C., Yang, L., Li, J., & Qian, D. (2016). A Novel and Facile One-Pot Solvothermal Synthesis of PEDOT-PSS/Ni-Mn-Co-O Hybrid as an Advanced Supercapacitor Electrode Material. ACS applied materials & interfaces, 8(4), 2741-52. https://doi.org/10.1021/acsami.5b11022
Yin, Chengjie, et al. "A Novel and Facile One-Pot Solvothermal Synthesis of PEDOT-PSS/Ni-Mn-Co-O Hybrid as an Advanced Supercapacitor Electrode Material." ACS applied materials & interfaces vol. 8,4 (2016): 2741-52. doi: https://doi.org/10.1021/acsami.5b11022
Yin C, Yang C, Jiang M, Deng C, Yang L, Li J, Qian D. A Novel and Facile One-Pot Solvothermal Synthesis of PEDOT-PSS/Ni-Mn-Co-O Hybrid as an Advanced Supercapacitor Electrode Material. ACS Appl Mater Interfaces. 2016 Feb 03;8(4):2741-52. doi: 10.1021/acsami.5b11022. Epub 2016 Jan 21. PMID: 26794146.
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Transparent conductive oxide-free perovskite solar cells with PEDOT:PSS as transparent electrode.

ACS applied materials & interfaces

Sun K, Li P, Xia Y, Chang J, Ouyang J.
PMID: 26132334
ACS Appl Mater Interfaces. 2015 Jul 22;7(28):15314-20. doi: 10.1021/acsami.5b03171. Epub 2015 Jul 10.

UNLABELLED: Perovskite solar cells (PSCs) have been attracting considerable attention because of their low fabrication cost and impressive energy conversion efficiency. Most PSCs are built on transparent conductive oxides (TCOs) such as fluorine-doped tin oxide (FTO) or indium tin...

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Sun K, Li P, Xia Y, et al. Transparent conductive oxide-free perovskite solar cells with PEDOT:PSS as transparent electrode. ACS Appl Mater Interfaces. 2015;7(28):15314-20doi: 10.1021/acsami.5b03171.
Sun, K., Li, P., Xia, Y., Chang, J., & Ouyang, J. (2015). Transparent conductive oxide-free perovskite solar cells with PEDOT:PSS as transparent electrode. ACS applied materials & interfaces, 7(28), 15314-20. https://doi.org/10.1021/acsami.5b03171
Sun, Kuan, et al. "Transparent conductive oxide-free perovskite solar cells with PEDOT:PSS as transparent electrode." ACS applied materials & interfaces vol. 7,28 (2015): 15314-20. doi: https://doi.org/10.1021/acsami.5b03171
Sun K, Li P, Xia Y, Chang J, Ouyang J. Transparent conductive oxide-free perovskite solar cells with PEDOT:PSS as transparent electrode. ACS Appl Mater Interfaces. 2015 Jul 22;7(28):15314-20. doi: 10.1021/acsami.5b03171. Epub 2015 Jul 10. PMID: 26132334.
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Evidence of simple intramolecular rearrangement at polymer end groups in secondary ion mass spectrometry.

Rapid communications in mass spectrometry : RCM

Eynde XV, Oike H, Hamada M, Tezuka Y, Bertrand P.
PMID: 10487938
Rapid Commun Mass Spectrom. 1999 Oct 15;13(19):1917-1923. doi: 10.1002/(SICI)1097-0231(19991015)13:19<1917::AID-RCM733>3.0.CO;2-P.

Polystyrenes with various end groups were analyzed by time-of-flight secondary ion mass spectrometry (TOF-SIMS). These end groups were obtained by termination of the active anionic group by sulfonate or chlorosilane derivatives. Characteristic end group fragments for each sulfonate derivative...

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Eynde XV, Oike H, Hamada M, et al. Evidence of simple intramolecular rearrangement at polymer end groups in secondary ion mass spectrometry. Rapid Commun Mass Spectrom. 1999;13(19):1917-1923doi: 10.1002/(SICI)1097-0231(19991015)13:19<1917::AID-RCM733>3.0.CO;2-P.
Eynde, X. V., Oike, H., Hamada, M., Tezuka, Y., & Bertrand, P. (1999). Evidence of simple intramolecular rearrangement at polymer end groups in secondary ion mass spectrometry. Rapid communications in mass spectrometry : RCM, 13(19), 1917-1923. https://doi.org/10.1002/(SICI)1097-0231(19991015)13:19<1917::AID-RCM733>3.0.CO;2-P
Eynde, et al. "Evidence of simple intramolecular rearrangement at polymer end groups in secondary ion mass spectrometry." Rapid communications in mass spectrometry : RCM vol. 13,19 (1999): 1917-1923. doi: https://doi.org/10.1002/(SICI)1097-0231(19991015)13:19<1917::AID-RCM733>3.0.CO;2-P
Eynde XV, Oike H, Hamada M, Tezuka Y, Bertrand P. Evidence of simple intramolecular rearrangement at polymer end groups in secondary ion mass spectrometry. Rapid Commun Mass Spectrom. 1999 Oct 15;13(19):1917-1923. doi: 10.1002/(SICI)1097-0231(19991015)13:19<1917::AID-RCM733>3.0.CO;2-P. PMID: 10487938.
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Polymer-coated ferromagnetic colloids from well-defined macromolecular surfactants and assembly into nanoparticle chains.

Journal of the American Chemical Society

Korth BD, Keng P, Shim I, Bowles SE, Tang C, Kowalewski T, Nebesny KW, Pyun J.
PMID: 16704248
J Am Chem Soc. 2006 May 24;128(20):6562-3. doi: 10.1021/ja0609147.

A novel synthetic route to polymer-coated ferromagnetic colloids of metallic cobalt has been developed. Well-defined end-functional polystyrenes were synthesized using controlled radical polymerization and used as surfactants in the thermolysis of dicobaltoctacarbonyl to afford uniform ferromagnetic nanoparticles. The presence...

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Korth BD, Keng P, Shim I, et al. Polymer-coated ferromagnetic colloids from well-defined macromolecular surfactants and assembly into nanoparticle chains. J Am Chem Soc. 2006;128(20):6562-3doi: 10.1021/ja0609147.
Korth, B. D., Keng, P., Shim, I., Bowles, S. E., Tang, C., Kowalewski, T., Nebesny, K. W., & Pyun, J. (2006). Polymer-coated ferromagnetic colloids from well-defined macromolecular surfactants and assembly into nanoparticle chains. Journal of the American Chemical Society, 128(20), 6562-3. https://doi.org/10.1021/ja0609147
Korth, Bryan D, et al. "Polymer-coated ferromagnetic colloids from well-defined macromolecular surfactants and assembly into nanoparticle chains." Journal of the American Chemical Society vol. 128,20 (2006): 6562-3. doi: https://doi.org/10.1021/ja0609147
Korth BD, Keng P, Shim I, Bowles SE, Tang C, Kowalewski T, Nebesny KW, Pyun J. Polymer-coated ferromagnetic colloids from well-defined macromolecular surfactants and assembly into nanoparticle chains. J Am Chem Soc. 2006 May 24;128(20):6562-3. doi: 10.1021/ja0609147. PMID: 16704248.
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Tandem mass spectrometry characteristics of silver-cationized polystyrenes: backbone degradation via free radical chemistry.

Analytical chemistry

Polce MJ, Ocampo M, Quirk RP, Wesdemiotis C.
PMID: 18085749
Anal Chem. 2008 Jan 15;80(2):347-54. doi: 10.1021/ac071071k. Epub 2007 Dec 18.

The [M + Ag](+) ions of polystyrene (PS) oligomers are formed by matrix-assisted laser desorption/ionization, and their fragmentation characteristics are determined by tandem mass spectrometry experiments in a quadrupole/time-of-flight mass spectrometer. Collisionally activated dissociation (CAD) of [M + Ag](+)...

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Polce MJ, Ocampo M, Quirk RP, et al. Tandem mass spectrometry characteristics of silver-cationized polystyrenes: backbone degradation via free radical chemistry. Anal Chem. 2007;80(2):347-54doi: 10.1021/ac071071k.
Polce, M. J., Ocampo, M., Quirk, R. P., & Wesdemiotis, C. (2008). Tandem mass spectrometry characteristics of silver-cationized polystyrenes: backbone degradation via free radical chemistry. Analytical chemistry, 80(2), 347-54. https://doi.org/10.1021/ac071071k
Polce, Michael J, et al. "Tandem mass spectrometry characteristics of silver-cationized polystyrenes: backbone degradation via free radical chemistry." Analytical chemistry vol. 80,2 (2008): 347-54. doi: https://doi.org/10.1021/ac071071k
Polce MJ, Ocampo M, Quirk RP, Wesdemiotis C. Tandem mass spectrometry characteristics of silver-cationized polystyrenes: backbone degradation via free radical chemistry. Anal Chem. 2008 Jan 15;80(2):347-54. doi: 10.1021/ac071071k. Epub 2007 Dec 18. PMID: 18085749.
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Allyl ansa-lanthanidocenes: single-component, single-site catalysts for controlled syndiospecific styrene and styrene-ethylene (Co)polymerization.

Chemistry (Weinheim an der Bergstrasse, Germany)

Rodrigues AS, Kirillov E, Lehmann CW, Roisnel T, Vuillemin B, Razavi A, Carpentier JF.
PMID: 17309082
Chemistry. 2007;13(19):5548-65. doi: 10.1002/chem.200601708.

A series of new neutral allyl Group 3 metal complexes bearing ansa-bridged fluorenyl/cyclopentadienyl ligands [[Flu-EMe(2)-(3-R-Cp)]Ln(eta(3)-C(3)H(5))(THF)] (E=C, R=H, Ln=Y (2), La (3), Nd (4), Sm (5); R=tBu, Ln=Y (8), Nd (9); E=Si, R=H, Ln=Y (12), Nd (13)) were synthesized in...

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Rodrigues AS, Kirillov E, Lehmann CW, et al. Allyl ansa-lanthanidocenes: single-component, single-site catalysts for controlled syndiospecific styrene and styrene-ethylene (Co)polymerization. Chemistry. 2007;13(19):5548-65doi: 10.1002/chem.200601708.
Rodrigues, A. S., Kirillov, E., Lehmann, C. W., Roisnel, T., Vuillemin, B., Razavi, A., & Carpentier, J. F. (2007). Allyl ansa-lanthanidocenes: single-component, single-site catalysts for controlled syndiospecific styrene and styrene-ethylene (Co)polymerization. Chemistry (Weinheim an der Bergstrasse, Germany), 13(19), 5548-65. https://doi.org/10.1002/chem.200601708
Rodrigues, Anne-Sophie, et al. "Allyl ansa-lanthanidocenes: single-component, single-site catalysts for controlled syndiospecific styrene and styrene-ethylene (Co)polymerization." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 13,19 (2007): 5548-65. doi: https://doi.org/10.1002/chem.200601708
Rodrigues AS, Kirillov E, Lehmann CW, Roisnel T, Vuillemin B, Razavi A, Carpentier JF. Allyl ansa-lanthanidocenes: single-component, single-site catalysts for controlled syndiospecific styrene and styrene-ethylene (Co)polymerization. Chemistry. 2007;13(19):5548-65. doi: 10.1002/chem.200601708. PMID: 17309082.
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Showing 1 to 12 of 228 entries