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Articoli di riviste sul tema "Macrophotoinitiator"

Autore: Grafiati

Pubblicato: 31 agosto 2024

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1

Jiang, Xuesong, Wenfeng Wang, Hongjie Xu e Jie Yin. "Water-compatible dendritic macrophotoinitiator containing thioxanthone". Journal of Photochemistry and Photobiology A: Chemistry 181, n. 2-3 (luglio 2006): 233–37. http://dx.doi.org/10.1016/j.jphotochem.2005.12.002.

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2

Jiang, Xuesong, e Jie Yin. "Dendritic Macrophotoinitiator Containing Thioxanthone and Coinitiator Amine". Macromolecules 37, n. 21 (ottobre 2004): 7850–53. http://dx.doi.org/10.1021/ma0488360.

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3

Ye, G. D., H. Zhou, J. W. Yang, Z. H. Zeng e Y. L. Chen. "Photoinitiating behavior of macrophotoinitiator containing aminoalkylphenone group". Journal of Thermal Analysis and Calorimetry 85, n. 3 (29 maggio 2006): 771–77. http://dx.doi.org/10.1007/s10973-005-7271-x.

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4

Kaya, N. U., A. Onen e Y. Guvenilir. "Photopolymerization of acrylates by enzymatically synthesized PCL based macrophotoinitiator". Express Polymer Letters 11, n. 6 (2017): 493–503. http://dx.doi.org/10.3144/expresspolymlett.2017.46.

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5

Wang, Sheng-Jie, Xiao-Dong Fan, Xiang Liu, Jie Kong, Yu-Yang Liu e Xin Wang. "Dendritic carbosilane-based macrophotoinitiator: synthesis, characterization, and photoinitiating behavior". Polymer International 56, n. 6 (2007): 764–72. http://dx.doi.org/10.1002/pi.2205.

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6

Ma, Zhengfeng, Xiling Niu, Zhihua Xu e Jinshan Guo. "Synthesis of novel macrophotoinitiator for the photopolymerization of acrylate". Journal of Applied Polymer Science 131, n. 11 (10 gennaio 2014): n/a. http://dx.doi.org/10.1002/app.40352.

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7

Jiang, Xuesong, e Jie Yin. "Study of macrophotoinitiator containing in-chain thioxanthone and coinitiator amines". Polymer 45, n. 15 (luglio 2004): 5057–63. http://dx.doi.org/10.1016/j.polymer.2004.05.050.

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8

Tan, Jianbo, Bo Wu, Jianwen Yang, Yedan Zhu e Zhaohua Zeng. "Photoinitiated dispersion polymerization using polyurethane based macrophotoinitiator as stabilizer and photoinitiator". Polymer 51, n. 15 (luglio 2010): 3394–401. http://dx.doi.org/10.1016/j.polymer.2010.05.052.

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9

Li, Shurun, Jianping Deng e Wantai Yang. "The preparation of amphiphilic core-shell nanospheres by using water-soluble macrophotoinitiator". Journal of Polymer Science Part A: Polymer Chemistry 48, n. 4 (12 gennaio 2010): 936–42. http://dx.doi.org/10.1002/pola.23849.

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10

Wei, Jun, e Fang Liu. "Novel Highly Efficient Macrophotoinitiator Comprising Benzophenone, Coinitiator Amine, and Thio Moieties for Photopolymerization". Macromolecules 42, n. 15 (11 agosto 2009): 5486–91. http://dx.doi.org/10.1021/ma900887h.

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11

Deka, S. R., e D. K. Kakati. "Benzoin-terminated polyurethane as macrophotoinitiator for synthesis of polyurethane-polymethyl methacrylate block copolymers". Journal of Applied Polymer Science 111, n. 6 (gennaio 2009): 3089–93. http://dx.doi.org/10.1002/app.29332.

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12

Ajayaghosh, A. "Macrophotoinitiator containing pendent xanthate chromophore: photopolymerization of methyl methacrylate and evaluation of kinetic parameters". Polymer 36, n. 10 (maggio 1995): 2049–53. http://dx.doi.org/10.1016/0032-3861(95)91451-c.

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13

Akat, H., e M. Ozkan. "Synthesis and characterization of poly(vinylchloride) type macrophotoinitiator comprising side-chain thioxanthone via click chemistry". Express Polymer Letters 5, n. 4 (2011): 318–26. http://dx.doi.org/10.3144/expresspolymlett.2011.32.

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14

Degirmenci, Mustafa. "Synthesis and Characterization of Novel Well‐Defined End‐Functional Macrophotoinitiator of Poly(MMA) by ATRP". Journal of Macromolecular Science, Part A 42, n. 1 (gennaio 2005): 21–30. http://dx.doi.org/10.1081/ma-200040949.

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15

Degirmenci, Mustafa, e Nasrettin Genli. "Synthesis of Well-Defined Telechelic Macrophotoinitiator of Polystyrene by Combination of ATRP and Click Chemistry". Macromolecular Chemistry and Physics 210, n. 19 (1 settembre 2009): 1617–23. http://dx.doi.org/10.1002/macp.200900221.

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16

Degirmenci, Mustafa. "Synthesis of Novel Well-defined End-functional Macrophotoinitiator of Poly(ε-caprolactone) by Ring-opening Polymerization". Polymer Journal 36, n. 7 (luglio 2004): 542–48. http://dx.doi.org/10.1295/polymj.36.542.

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17

Degirmenci, Mustafa, Edip Taskesen, Sirin Hicri e Hasim Yilmaz. "Synthesis and characterization of a novel mid‐chain macrophotoinitiator of polyacrylonitrile by Ce(IV)/HNO3redox system". Journal of Polymer Science Part A: Polymer Chemistry 46, n. 16 (15 agosto 2008): 5404–13. http://dx.doi.org/10.1002/pola.22860.

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18

Körpınar, Berna, Fehmi Saltan, Hakan Akat e Armağan Kınal. "Synthesis, characterization and computational investigation of poly(styrene-co-1-methylpyrenyl methacrylate): its efficiency as a macrophotoinitiator". International Journal of Polymer Analysis and Characterization 25, n. 3 (2 aprile 2020): 134–46. http://dx.doi.org/10.1080/1023666x.2020.1766787.

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19

Wei, Jun, Hongyu Wang, Xuesong Jiang e Jie Yin. "Novel Photosensitive Thio-Containing Polyurethane as Macrophotoinitiator Comprising Side-Chain Benzophenone and Co-Initiator Amine for Photopolymerization". Macromolecules 40, n. 7 (aprile 2007): 2344–51. http://dx.doi.org/10.1021/ma0615304.

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20

Niwa, Masazo, Yasuhiro Sako e Motoyuki Shimizu. "Block Polymerizations of Vinyl Monomers Initiated by Telechelicisopropyl Xanthate-Terminated Polymers as Macrophotoinitiator. Design Of Block Copolymers. 2". Journal of Macromolecular Science: Part A - Chemistry 24, n. 11 (1 novembre 1987): 1315–32. http://dx.doi.org/10.1080/00222338708076948.

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21

Degirmenci, Mustafa, Mehmet Akif Sarac e Nasrettin Genli. "Synthesis and characterization of mid-chain macrophotoinitiator of poly(ε-caprolactone) by combination of ROP and click chemistry". Polymer Bulletin 71, n. 7 (8 maggio 2014): 1743–55. http://dx.doi.org/10.1007/s00289-014-1152-z.

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22

Degirmenci, Mustafa, Mehmet Ali Akbulut, Sirin Hicri e Hasim Yilmaz. "Synthesis and Characterization of a Novel Mid-Chain Macrophotoinitiator of Poly(methyl methacrylate) by Ce(IV)/HNO3 Redox System". Polymer Journal 40, n. 8 (18 giugno 2008): 729–35. http://dx.doi.org/10.1295/polymj.pj2008060.

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23

Degirmenci, Mustafa, Sirin Hicri e Hasim Yilmaz. "Synthesis and characterization of a novel water-soluble mid-chain macrophotoinitiator of polyacrylamide by Ce(IV)/HNO3 redox system". European Polymer Journal 44, n. 11 (novembre 2008): 3776–81. http://dx.doi.org/10.1016/j.eurpolymj.2008.08.008.

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24

Poly, Julien, Benjamin Cabannes-Boué, Laura Hebinger, Rémy Mangin, Aurore Sauvage, Pu Xiao, Fabrice Morlet-Savary e Jacques Lalevée. "Polymers synthesized by RAFT as versatile macrophotoinitiators". Polymer Chemistry 6, n. 31 (2015): 5766–72. http://dx.doi.org/10.1039/c5py00608b.

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25

Jiang, Xuesong, Hongjie Xu e Jie Yin. "Copolymeric dendritic macrophotoinitiators". Polymer 46, n. 24 (novembre 2005): 11079–84. http://dx.doi.org/10.1016/j.polymer.2005.09.014.

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26

Kaastrup, K., e H. D. Sikes. "Investigation of dendrimers functionalized with eosin as macrophotoinitiators for polymerization-based signal amplification reactions". RSC Advances 5, n. 20 (2015): 15652–59. http://dx.doi.org/10.1039/c4ra14466j.

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27

Degirmenci, Mustafa, Cafer Gokkaya e Mustafa Durgun. "One-step synthesis of a mid-chain functional macrophotoinitiator of a polystyrene-poly(ɛ-caprolactone) diblock copolymer via simultaneous ATRP and ROP using a dual-functional photoinitiator". Polymer Journal 48, n. 2 (4 novembre 2015): 139–45. http://dx.doi.org/10.1038/pj.2015.93.

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28

Tehfe, Mohamad-Ali, Jacques Lalevée, Ravi Shankar, Usharani Sahoo, Fabrice Morlet-Savary, Bernadette Graff e Jean-Pierre Fouassier. "Branched and Network Polysilanes as Cleavable Macrophotoinitiators". Macromolecular Chemistry and Physics 212, n. 24 (18 ottobre 2011): 2619–25. http://dx.doi.org/10.1002/macp.201100440.

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29

Uyar, Zafer, Mustafa Degirmenci, Nasrettin Genli e Ayse Yilmaz. "Synthesis of well-defined bisbenzoin end-functionalized poly(ε-caprolactone) macrophotoinitiator by combination of ROP and click chemistry and its use in the synthesis of star copolymers by photoinduced free radical promoted cationic polymerization". Designed Monomers and Polymers 20, n. 1 (20 settembre 2016): 42–53. http://dx.doi.org/10.1080/15685551.2016.1231041.

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30

Degirmenci, Mustafa, Nalan Benek e Mustafa Durgun. "Synthesis of benzoin end-chain functional macrophotoinitiator of poly(d,l-lactide) homopolymer and poly(ε-caprolactone)-poly(d,l-lactide) diblock copolymer by ROP and their use in photoinduced free radical promoted cationic copolymerization". Polymer Bulletin 74, n. 1 (30 maggio 2016): 167–81. http://dx.doi.org/10.1007/s00289-016-1706-3.

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31

Corrales, T., F. Catalina, C. Peinado e N. S. Allen. "Free radical macrophotoinitiators: an overview on recent advances". Journal of Photochemistry and Photobiology A: Chemistry 159, n. 2 (luglio 2003): 103–14. http://dx.doi.org/10.1016/s1010-6030(03)00175-8.

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32

Fan, Yunxin, Yan Song, Na He, Fei Cheng, Xiaojiao Jiao, Guoqiao Lai, Xilin Hua e Xiongfa Yang. "High Efficiency and Low Migration Hyperbranched Silicone Contain Macrophotoinitiators for UV-Cured Transparent Coatings". Polymers 12, n. 12 (16 dicembre 2020): 3005. http://dx.doi.org/10.3390/polym12123005.

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Abstract (sommario):

A kind of hyperbranched silicone containing macrophotoinitiators (HBSMIs) were synthesized from 2-hydroxy-2-methyl-1-phenyl propanone (HMPP) and the UV-curing behaviors of HBSMIs were investigated in UV-cured transparent polyurethane-acrylate (PUA) coatings. HBSMIs show higher UV-initiating efficiency than HMPP. The migration of HBSMIs from the UV-cured coatings can be as low as 1.7–6.0 wt%, which is obviously lower than the migration of HMPP. There is a remarkable improvement of the tensile strength of the UV-cured materials initiated by HBSMI in comparison to that of the materials prepared with the same PUA initiated by HMPP. Especially for the UV-cured materials prepared from PUA with 20 wt% 1,1,1-tris(hydroxymethyl)propane (TMP), the tensile strength and the strain at break increased from 6.81 MPa to 12.14 MPa and from 43.0% to 71.9%, respectively. The fraction of improvement for the tensile strength and the strain at break is as high as 78.9% and 67.2%, respectively. The coatings prepared with HBSMI also have better UV resistance ability than those coatings prepared with HMPP because they turn slightly yellow when they are aged by UV for about 15 min while the coating prepared with 4 wt% of HMPP will turn yellow only aged by UV for 2 min. These results suggest that preparation hyperbranched silicone containing macrophotoinitiators will be one of the good strategies to improve the curing efficiency of the UV-curing system, reduce the migration of UV initiator from cured material, improve the mechanical and UV resistance performance of UV-cured materials.

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33

Lee, Jungkyu K., Brandon W. Heimer e Hadley D. Sikes. "Systematic Study of Fluorescein-Functionalized Macrophotoinitiators for Colorimetric Bioassays". Biomacromolecules 13, n. 4 (22 marzo 2012): 1136–43. http://dx.doi.org/10.1021/bm300037t.

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34

Sandmeier, Matthias, Nevena Paunović, Riccardo Conti, Leopold Hofmann, Jieping Wang, Zhi Luo, Kunal Masania et al. "Solvent-Free Three-Dimensional Printing of Biodegradable Elastomers Using Liquid Macrophotoinitiators". Macromolecules 54, n. 17 (23 agosto 2021): 7830–39. http://dx.doi.org/10.1021/acs.macromol.1c00856.

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35

Degirmenci, Mustafa, Ioan Cianga e Yusuf Yagci. "Synthesis of well-defined polystyrene macrophotoinitiators by atom-transfer radical polymerization". Macromolecular Chemistry and Physics 203, n. 10-11 (luglio 2002): 1279–84. http://dx.doi.org/10.1002/1521-3935(200207)203:10/11<1279::aid-macp1279>3.0.co;2-h.

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36

Ohar, Halyna, Larysa Dolynska e Viktor Tokarev. "Synthesis and Application of Macrophotoinitiators Obtained via Benzoin Tethering with Copolymers of Maleic Anhydride". Chemistry & Chemical Technology 7, n. 2 (10 giugno 2013): 125–30. http://dx.doi.org/10.23939/chcht07.02.125.

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37

Degirmenci, Mustafa, Gurkan Hizal e Yusuf Yagci. "Synthesis and Characterization of Macrophotoinitiators of Poly(ε-caprolactone) and Their Use in Block Copolymerization". Macromolecules 35, n. 22 (ottobre 2002): 8265–70. http://dx.doi.org/10.1021/ma020668t.

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38

Yang, Jianjing, Can Xu, Wen Liao, Ying Xiong, Xiaoling Wang e Hongding Tang. "Visible macrophotoinitiators with Si-H: High efficient anti-oxygen inhibition and modified cured polymer materials". Progress in Organic Coatings 138 (gennaio 2020): 105410. http://dx.doi.org/10.1016/j.porgcoat.2019.105410.

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39

Wu, Qingqing, Wen Liao, Xiaoling Wang, Ying Xiong e Hongding Tang. "Sole‐Component Visible Macrophotoinitiators with Si‐H: Decreased Oxygen Inhibition and Modified Cured Polymer Materials". ChemistrySelect 5, n. 33 (3 settembre 2020): 10243–49. http://dx.doi.org/10.1002/slct.202001069.

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40

Baralle, Alexandre, Patxi Garra, Bernadette Graff, Fabrice Morlet-Savary, Céline Dietlin, Jean Pierre Fouassier, Sami Lakhdar e Jacques Lalevée. "Iodinated Polystyrene for Polymeric Charge Transfer Complexes: Toward High-Performance Near-UV and Visible Light Macrophotoinitiators". Macromolecules 52, n. 9 (29 aprile 2019): 3448–53. http://dx.doi.org/10.1021/acs.macromol.9b00252.

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41

Cakmak, Ismail, e Temel Ozturk. "Synthesis of Triblock Copolymers via Photopolymerization of Styrene and Methyl Methacrylate Using Macrophotoinitiators Possessing Poly(ethylene glycol) Units". Journal of Polymer Research 12, n. 2 (aprile 2005): 121–26. http://dx.doi.org/10.1007/s10965-004-2935-y.

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42

Uyar, Zafer, Ferhat Turgut, Ulku Arslan, Mustafa Durgun e Mustafa Degirmenci. "Synthesis and characterization of well-defined end-chain functional macrophotoinitiators of polystyrene and polyacrylonitrile by RAFT/MADIX polymerization". European Polymer Journal 119 (ottobre 2019): 102–13. http://dx.doi.org/10.1016/j.eurpolymj.2019.07.028.

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43

Degirmenci, Mustafa, Selma Alter e Nasrettin Genli. "Synthesis and Characterization of Well-Defined Mid-Chain Functional Macrophotoinitiators of Polystyrene by Combination of ATRP and “Click” Chemistry". Macromolecular Chemistry and Physics 212, n. 15 (28 giugno 2011): 1575–81. http://dx.doi.org/10.1002/macp.201100116.

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44

Yilmaz, Hasim, Mustafa Degirmenci, Ümmihan Yilmaz e Halil Ibrahim Unal. "End-chain and Mid-chain Functional Macrophotoinitiators of Poly(ε-caprolactone) and Their Molar Mass Effects on Strong Electrorheological Response". Polymer Journal 39, n. 1 (24 novembre 2006): 24–33. http://dx.doi.org/10.1295/polymj.pj2006048.

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45

Degirmenci, Mustafa, Tuba Urun, Mustafa Durgun e Esra Barim. "Synthesis of mid-chain functional macrophotoinitiators of poly(D,L-lactide) homopolymer and tetrablock poly(D,L-lactide)-poly(ε-caprolactone) copolymer by ring-opening polymerization". Designed Monomers and Polymers 18, n. 7 (30 luglio 2015): 669–77. http://dx.doi.org/10.1080/15685551.2015.1070499.

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46

Cakmak, Ismail, e Temel Ozturk. "Correction: Synthesis of Triblock Copolymers via Photoplymerization of Styrene and Methyl Methacrylate Using Macrophotoinitiators Possessing Poly(ethylene glycol) Units. Journal of Polymer Research, (2005) 12: 121–126". Journal of Polymer Research 13, n. 3 (4 marzo 2006): 255. http://dx.doi.org/10.1007/s10965-006-9043-0.

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47

Uyar, Zafer, Mustafa Durgun, M. Sukru Yavuz, M. Bahattin Abaci, Ulku Arslan e Mustafa Degirmenci. "Two-arm PCL and PLLA macrophotoinitiators with benzoin end-functional groups by combination of ROP and click chemistry and their use in the synthesis of A2B2 type miktoarm star copolymers". Polymer 123 (agosto 2017): 153–68. http://dx.doi.org/10.1016/j.polymer.2017.07.019.

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48

Xie, Yangzhi, e He Huang. "Preparation and characterization of an amphiphilic macrophotoinitiator based on 2-hydroxyl-2-methyl-1-phenylpropanone". Journal of Applied Polymer Science 133, n. 36 (4 giugno 2016). http://dx.doi.org/10.1002/app.43910.

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49

Uyar, Zafer, e Emel Kaya. "Synthesis of an (AB)4-type Star Block Copolymer of L-lactide and Cyclohexene Oxide from a Tetra-Arm Telechelic Macrophotoinitiator". Journal of the Turkish Chemical Society, Section A: Chemistry, 22 settembre 2018, 1105–18. http://dx.doi.org/10.18596/jotcsa.450986.

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50

Degirmenci, Mustafa, Pinar Atuk Besli e Nasrettin Genli. "Synthesis of a well-defined end-chain macrophotoinitiator of poly(ε − caprolactone) by combination of ring-opening polymerization and click chemistry". Journal of Polymer Research 21, n. 9 (7 agosto 2014). http://dx.doi.org/10.1007/s10965-014-0540-2.

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