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Journal articles on the topic 'Macrophotoinitiator'

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1

Jiang, Xuesong, Wenfeng Wang, Hongjie Xu, and Jie Yin. "Water-compatible dendritic macrophotoinitiator containing thioxanthone." Journal of Photochemistry and Photobiology A: Chemistry 181, no. 2-3 (July 2006): 233–37. http://dx.doi.org/10.1016/j.jphotochem.2005.12.002.

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2

Jiang, Xuesong, and Jie Yin. "Dendritic Macrophotoinitiator Containing Thioxanthone and Coinitiator Amine." Macromolecules 37, no. 21 (October 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, and Y. L. Chen. "Photoinitiating behavior of macrophotoinitiator containing aminoalkylphenone group." Journal of Thermal Analysis and Calorimetry 85, no. 3 (May 29, 2006): 771–77. http://dx.doi.org/10.1007/s10973-005-7271-x.

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4

Kaya, N. U., A. Onen, and Y. Guvenilir. "Photopolymerization of acrylates by enzymatically synthesized PCL based macrophotoinitiator." Express Polymer Letters 11, no. 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, and Xin Wang. "Dendritic carbosilane-based macrophotoinitiator: synthesis, characterization, and photoinitiating behavior." Polymer International 56, no. 6 (2007): 764–72. http://dx.doi.org/10.1002/pi.2205.

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6

Ma, Zhengfeng, Xiling Niu, Zhihua Xu, and Jinshan Guo. "Synthesis of novel macrophotoinitiator for the photopolymerization of acrylate." Journal of Applied Polymer Science 131, no. 11 (January 10, 2014): n/a. http://dx.doi.org/10.1002/app.40352.

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7

Jiang, Xuesong, and Jie Yin. "Study of macrophotoinitiator containing in-chain thioxanthone and coinitiator amines." Polymer 45, no. 15 (July 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, and Zhaohua Zeng. "Photoinitiated dispersion polymerization using polyurethane based macrophotoinitiator as stabilizer and photoinitiator." Polymer 51, no. 15 (July 2010): 3394–401. http://dx.doi.org/10.1016/j.polymer.2010.05.052.

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9

Li, Shurun, Jianping Deng, and Wantai Yang. "The preparation of amphiphilic core-shell nanospheres by using water-soluble macrophotoinitiator." Journal of Polymer Science Part A: Polymer Chemistry 48, no. 4 (January 12, 2010): 936–42. http://dx.doi.org/10.1002/pola.23849.

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10

Wei, Jun, and Fang Liu. "Novel Highly Efficient Macrophotoinitiator Comprising Benzophenone, Coinitiator Amine, and Thio Moieties for Photopolymerization." Macromolecules 42, no. 15 (August 11, 2009): 5486–91. http://dx.doi.org/10.1021/ma900887h.

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11

Deka, S. R., and D. K. Kakati. "Benzoin-terminated polyurethane as macrophotoinitiator for synthesis of polyurethane-polymethyl methacrylate block copolymers." Journal of Applied Polymer Science 111, no. 6 (January 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, no. 10 (May 1995): 2049–53. http://dx.doi.org/10.1016/0032-3861(95)91451-c.

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13

Akat, H., and M. Ozkan. "Synthesis and characterization of poly(vinylchloride) type macrophotoinitiator comprising side-chain thioxanthone via click chemistry." Express Polymer Letters 5, no. 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, no. 1 (January 2005): 21–30. http://dx.doi.org/10.1081/ma-200040949.

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15

Degirmenci, Mustafa, and Nasrettin Genli. "Synthesis of Well-Defined Telechelic Macrophotoinitiator of Polystyrene by Combination of ATRP and Click Chemistry." Macromolecular Chemistry and Physics 210, no. 19 (September 1, 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, no. 7 (July 2004): 542–48. http://dx.doi.org/10.1295/polymj.36.542.

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17

Degirmenci, Mustafa, Edip Taskesen, Sirin Hicri, and 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, no. 16 (August 15, 2008): 5404–13. http://dx.doi.org/10.1002/pola.22860.

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18

Körpınar, Berna, Fehmi Saltan, Hakan Akat, and 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, no. 3 (April 2, 2020): 134–46. http://dx.doi.org/10.1080/1023666x.2020.1766787.

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19

Wei, Jun, Hongyu Wang, Xuesong Jiang, and Jie Yin. "Novel Photosensitive Thio-Containing Polyurethane as Macrophotoinitiator Comprising Side-Chain Benzophenone and Co-Initiator Amine for Photopolymerization." Macromolecules 40, no. 7 (April 2007): 2344–51. http://dx.doi.org/10.1021/ma0615304.

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20

Niwa, Masazo, Yasuhiro Sako, and 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, no. 11 (November 1, 1987): 1315–32. http://dx.doi.org/10.1080/00222338708076948.

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21

Degirmenci, Mustafa, Mehmet Akif Sarac, and Nasrettin Genli. "Synthesis and characterization of mid-chain macrophotoinitiator of poly(ε-caprolactone) by combination of ROP and click chemistry." Polymer Bulletin 71, no. 7 (May 8, 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, and Hasim Yilmaz. "Synthesis and Characterization of a Novel Mid-Chain Macrophotoinitiator of Poly(methyl methacrylate) by Ce(IV)/HNO3 Redox System." Polymer Journal 40, no. 8 (June 18, 2008): 729–35. http://dx.doi.org/10.1295/polymj.pj2008060.

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23

Degirmenci, Mustafa, Sirin Hicri, and 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, no. 11 (November 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, and Jacques Lalevée. "Polymers synthesized by RAFT as versatile macrophotoinitiators." Polymer Chemistry 6, no. 31 (2015): 5766–72. http://dx.doi.org/10.1039/c5py00608b.

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25

Jiang, Xuesong, Hongjie Xu, and Jie Yin. "Copolymeric dendritic macrophotoinitiators." Polymer 46, no. 24 (November 2005): 11079–84. http://dx.doi.org/10.1016/j.polymer.2005.09.014.

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26

Kaastrup, K., and H. D. Sikes. "Investigation of dendrimers functionalized with eosin as macrophotoinitiators for polymerization-based signal amplification reactions." RSC Advances 5, no. 20 (2015): 15652–59. http://dx.doi.org/10.1039/c4ra14466j.

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27

Degirmenci, Mustafa, Cafer Gokkaya, and 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, no. 2 (November 4, 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, and Jean-Pierre Fouassier. "Branched and Network Polysilanes as Cleavable Macrophotoinitiators." Macromolecular Chemistry and Physics 212, no. 24 (October 18, 2011): 2619–25. http://dx.doi.org/10.1002/macp.201100440.

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29

Uyar, Zafer, Mustafa Degirmenci, Nasrettin Genli, and 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, no. 1 (September 20, 2016): 42–53. http://dx.doi.org/10.1080/15685551.2016.1231041.

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30

Degirmenci, Mustafa, Nalan Benek, and 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, no. 1 (May 30, 2016): 167–81. http://dx.doi.org/10.1007/s00289-016-1706-3.

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31

Corrales, T., F. Catalina, C. Peinado, and N. S. Allen. "Free radical macrophotoinitiators: an overview on recent advances." Journal of Photochemistry and Photobiology A: Chemistry 159, no. 2 (July 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, and Xiongfa Yang. "High Efficiency and Low Migration Hyperbranched Silicone Contain Macrophotoinitiators for UV-Cured Transparent Coatings." Polymers 12, no. 12 (December 16, 2020): 3005. http://dx.doi.org/10.3390/polym12123005.

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Abstract:
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, and Hadley D. Sikes. "Systematic Study of Fluorescein-Functionalized Macrophotoinitiators for Colorimetric Bioassays." Biomacromolecules 13, no. 4 (March 22, 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, no. 17 (August 23, 2021): 7830–39. http://dx.doi.org/10.1021/acs.macromol.1c00856.

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35

Degirmenci, Mustafa, Ioan Cianga, and Yusuf Yagci. "Synthesis of well-defined polystyrene macrophotoinitiators by atom-transfer radical polymerization." Macromolecular Chemistry and Physics 203, no. 10-11 (July 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, and Viktor Tokarev. "Synthesis and Application of Macrophotoinitiators Obtained via Benzoin Tethering with Copolymers of Maleic Anhydride." Chemistry & Chemical Technology 7, no. 2 (June 10, 2013): 125–30. http://dx.doi.org/10.23939/chcht07.02.125.

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37

Degirmenci, Mustafa, Gurkan Hizal, and Yusuf Yagci. "Synthesis and Characterization of Macrophotoinitiators of Poly(ε-caprolactone) and Their Use in Block Copolymerization." Macromolecules 35, no. 22 (October 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, and Hongding Tang. "Visible macrophotoinitiators with Si-H: High efficient anti-oxygen inhibition and modified cured polymer materials." Progress in Organic Coatings 138 (January 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, and Hongding Tang. "Sole‐Component Visible Macrophotoinitiators with Si‐H: Decreased Oxygen Inhibition and Modified Cured Polymer Materials." ChemistrySelect 5, no. 33 (September 3, 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, and Jacques Lalevée. "Iodinated Polystyrene for Polymeric Charge Transfer Complexes: Toward High-Performance Near-UV and Visible Light Macrophotoinitiators." Macromolecules 52, no. 9 (April 29, 2019): 3448–53. http://dx.doi.org/10.1021/acs.macromol.9b00252.

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41

Cakmak, Ismail, and 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, no. 2 (April 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, and Mustafa Degirmenci. "Synthesis and characterization of well-defined end-chain functional macrophotoinitiators of polystyrene and polyacrylonitrile by RAFT/MADIX polymerization." European Polymer Journal 119 (October 2019): 102–13. http://dx.doi.org/10.1016/j.eurpolymj.2019.07.028.

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43

Degirmenci, Mustafa, Selma Alter, and 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, no. 15 (June 28, 2011): 1575–81. http://dx.doi.org/10.1002/macp.201100116.

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44

Yilmaz, Hasim, Mustafa Degirmenci, Ümmihan Yilmaz, and 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, no. 1 (November 24, 2006): 24–33. http://dx.doi.org/10.1295/polymj.pj2006048.

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45

Degirmenci, Mustafa, Tuba Urun, Mustafa Durgun, and 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, no. 7 (July 30, 2015): 669–77. http://dx.doi.org/10.1080/15685551.2015.1070499.

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46

Cakmak, Ismail, and 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, no. 3 (March 4, 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, and 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 (August 2017): 153–68. http://dx.doi.org/10.1016/j.polymer.2017.07.019.

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48

Xie, Yangzhi, and He Huang. "Preparation and characterization of an amphiphilic macrophotoinitiator based on 2-hydroxyl-2-methyl-1-phenylpropanone." Journal of Applied Polymer Science 133, no. 36 (June 4, 2016). http://dx.doi.org/10.1002/app.43910.

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49

Uyar, Zafer, and 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, September 22, 2018, 1105–18. http://dx.doi.org/10.18596/jotcsa.450986.

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50

Degirmenci, Mustafa, Pinar Atuk Besli, and 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, no. 9 (August 7, 2014). http://dx.doi.org/10.1007/s10965-014-0540-2.

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