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1

Kim, Young H. "Highly branched polymers." Advanced Materials 4, no. 11 (1992): 764–66. http://dx.doi.org/10.1002/adma.19920041116.

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2

Yeagle, P. "Highly branched polymers deliver." Science 352, no. 6293 (2016): 1530–32. http://dx.doi.org/10.1126/science.352.6293.1530-u.

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3

Al-Kaysi, Rabih O., Fei Tong, Maram Al-Haidar, Lingyan Zhu, and Christopher J. Bardeen. "Highly branched photomechanical crystals." Chemical Communications 53, no. 17 (2017): 2622–25. http://dx.doi.org/10.1039/c6cc08999b.

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4

Rodríguez-Hernández, Juan, Marco Gatti, and Harm-Anton Klok. "Highly Branched Poly(l-lysine)." Biomacromolecules 4, no. 2 (2003): 249–58. http://dx.doi.org/10.1021/bm020096k.

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5

KIM, Y. H. "ChemInform Abstract: Highly Branched Polymers." ChemInform 24, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.199317270.

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6

Maciejewski, Mieczysław, Michał Kędzierski, Elżbieta Bednarek, and Ewa Rudnik. "Highly branched melamine-phenolic novolaks." Polymer Bulletin 48, no. 3 (2002): 251–59. http://dx.doi.org/10.1007/s00289-002-0030-2.

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7

Backinowsky, L. V., P. I. Abronina, S. A. Nepogodiev, A. A. Grachev, and N. K. Kochetkov. "Synthesis of highly branched oligomannosides." Russian Chemical Bulletin 47, no. 8 (1998): 1589–94. http://dx.doi.org/10.1007/bf02495616.

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8

Liao, Mengchen, Yang Chen, and Michael A. Brook. "Spatially Controlled Highly Branched Vinylsilicones." Polymers 13, no. 6 (2021): 859. http://dx.doi.org/10.3390/polym13060859.

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Branched silicones possess interesting properties as oils, including their viscoelastic behavior, or as precursors to controlled networks. However, highly branched silicone polymers are difficult to form reliably using a “grafting to” strategy because functional groups may be bunched together preventing complete conversion for steric reasons. We report the synthesis of vinyl-functional highly branched silicone polymers based, at their core, on the ability to spatially locate functional vinyl groups along a silicone backbone at the desired frequency. Macromonomers were created and then polymeri
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9

Mańczyk, Krzysztof, and Paweł Szewczyk. "Highly branched high solids alkyd resins." Progress in Organic Coatings 44, no. 2 (2002): 99–109. http://dx.doi.org/10.1016/s0300-9440(01)00249-1.

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10

Guo, Ke, Ying Liu, Min Han, Dongdong Xu, and Jianchun Bao. "Highly branched ultrathin Pt–Ru nanodendrites." Chemical Communications 55, no. 74 (2019): 11131–34. http://dx.doi.org/10.1039/c9cc05686f.

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11

Lim, Byungkwon, and Younan Xia. "Metal Nanocrystals with Highly Branched Morphologies." Angewandte Chemie International Edition 50, no. 1 (2010): 76–85. http://dx.doi.org/10.1002/anie.201002024.

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12

Roovers, Jacques. "Melt rheology of highly branched polymers." Journal of Non-Crystalline Solids 131-133 (June 1991): 793–98. http://dx.doi.org/10.1016/0022-3093(91)90683-w.

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13

Canning, Sarah L., Joseph M. F. Ferner, Natalie M. Mangham, et al. "Highly-ordered onion micelles made from amphiphilic highly-branched copolymers." Polymer Chemistry 9, no. 47 (2018): 5617–29. http://dx.doi.org/10.1039/c8py00800k.

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14

Jing, Shengchang, Xueli Guo, and Yiwei Tan. "Branched Pd and Pd-based trimetallic nanocrystals with highly open structures for methanol electrooxidation." Journal of Materials Chemistry A 4, no. 20 (2016): 7950–61. http://dx.doi.org/10.1039/c5ta10046a.

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Branched Pd and Pd-based trimetallic nanocrystals with long, thin branches and open structures were synthesized in high yields, which provides an avenue to developing high performance catalysts for methanol electrooxidation.
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15

Li, Taohong, Bengang Zhang, Shuyang Jiang, et al. "Novel Highly Branched Polymer Wood Adhesive Resin." ACS Sustainable Chemistry & Engineering 8, no. 13 (2020): 5209–16. http://dx.doi.org/10.1021/acssuschemeng.9b07732.

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16

England, Richard Mark, and Stephen Rimmer. "Hyper/highly-branched polymers by radical polymerisations." Polymer Chemistry 1, no. 10 (2010): 1533. http://dx.doi.org/10.1039/c0py00154f.

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17

Skorotetcky, M. S., O. V. Borshchev, N. M. Surin, and S. A. Ponomarenko. "Novel highly efficient blue-emitting branched oligoarylsilanes." Journal of Physics: Conference Series 1124 (December 2018): 051010. http://dx.doi.org/10.1088/1742-6596/1124/5/051010.

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18

Tao, Wei, and Lifeng Yan. "Thermogelling of highly branched poly(N-isopropylacrylamide)." Journal of Applied Polymer Science 118, no. 6 (2010): 3391–99. http://dx.doi.org/10.1002/app.32410.

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19

Cuneo, Timothy, Robert W. Graff, Xiaofeng Wang, and Haifeng Gao. "Synthesis of Highly Branched Copolymers in Microemulsion." Macromolecular Chemistry and Physics 220, no. 6 (2019): 1800546. http://dx.doi.org/10.1002/macp.201800546.

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20

Munari, A., G. Pezzin, F. Pilati, and P. Manaresi. "Rheological characterization of highly branched poly(ethyleneterephthalate)." Rheologica Acta 28, no. 1 (1989): 25–29. http://dx.doi.org/10.1007/bf01354765.

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21

Jiang, Shuyang, Mengyang Hu, Guanben Du, Zhigang Duan, Xiaojian Zhou, and Taohong Li. "Highly Branched Polyurea-Enhanced Urea-Formaldehyde Resin." ACS Applied Polymer Materials 3, no. 2 (2021): 1157–70. http://dx.doi.org/10.1021/acsapm.0c01362.

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22

Kurochkin, S. A., L. I. Makhonina, S. G. Vasil’ev, et al. "Hydrodynamic characteristics of branched polystyrenes with varying content of a highly branched fraction." Polymer Science, Series A 59, no. 5 (2017): 613–23. http://dx.doi.org/10.1134/s0965545x17050078.

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23

Hubbard, Lauren, Paula McSteen, John Doebley, and Sarah Hake. "Expression Patterns and Mutant Phenotype of teosinte branched1 Correlate With Growth Suppression in Maize and Teosinte." Genetics 162, no. 4 (2002): 1927–35. http://dx.doi.org/10.1093/genetics/162.4.1927.

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Abstract The evolution of domesticated maize from its wild ancestor teosinte is a dramatic example of the effect of human selection on agricultural crops. Maize has one dominant axis of growth, whereas teosinte is highly branched. The axillary branches in maize are short and feminized whereas the axillary branches of teosinte are long and end in a male inflorescence under normal growth conditions. Previous QTL and molecular analysis suggested that the teosinte branched1 (tb1) gene of maize contributed to the architectural difference between maize and teosinte. tb1 mutants of maize resemble teo
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24

Robson, J. N., and S. J. Rowland. "Synthesis of a highly branched C30 sedimentary hydrocarbon." Tetrahedron Letters 29, no. 31 (1988): 3837–40. http://dx.doi.org/10.1016/s0040-4039(00)82128-0.

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25

Wang, C., M. C. Chu, T. L. Lin, S. M. Lai, H. H. Shih, and J. C. Yang. "Microstructures of a highly short-chain branched polyethylene." Polymer 42, no. 4 (2001): 1733–41. http://dx.doi.org/10.1016/s0032-3861(00)00566-8.

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26

Trollsås, Mikael, Melissa A. Kelly, Hans Claesson, Richard Siemens, and James L. Hedrick. "Highly Branched Block Copolymers: Design, Synthesis, and Morphology." Macromolecules 32, no. 15 (1999): 4917–24. http://dx.doi.org/10.1021/ma990054x.

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27

Auh, J. H., H. G. Lee, J. W. Kim, J. C. Kim, H. S. Yoon, and K. H. Park. "Highly Concentrated Branched Oligosaccharides as Cryoprotectant for Surimi." Journal of Food Science 64, no. 3 (1999): 418–22. http://dx.doi.org/10.1111/j.1365-2621.1999.tb15055.x.

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28

Lim, Byungkwon, and Younan Xia. "ChemInform Abstract: Metal Nanocrystals with Highly Branched Morphologies." ChemInform 42, no. 13 (2011): no. http://dx.doi.org/10.1002/chin.201113226.

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29

Belt, Simon T., W. Guy Allard, Lesley Johns, et al. "Variable stereochemistry in highly branched isoprenoids from diatoms." Chirality 13, no. 8 (2001): 415–19. http://dx.doi.org/10.1002/chir.1053.

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30

Chickos, James S., Donald G. Hesse, Sarah Hosseini, et al. "Enthalpies of vaporization of some highly branched hydrocarbons." Journal of Chemical Thermodynamics 27, no. 6 (1995): 693–705. http://dx.doi.org/10.1006/jcht.1995.0071.

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31

Auh, J. H., Y. R. Kim, P. Cornillon, J. Yoon, S. H. Yoo, and K. H. Park. "Cryoprotection of protein by highly concentrated branched oligosaccharides." International Journal of Food Science and Technology 38, no. 5 (2003): 553–63. http://dx.doi.org/10.1046/j.1365-2621.2003.00694.x.

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32

Braunecker, Wade A., Akin Akdag, Byron A. Boon, and Josef Michl. "Highly Branched Polypropylene via Li+-Catalyzed Radical Polymerization." Macromolecules 44, no. 6 (2011): 1229–32. http://dx.doi.org/10.1021/ma102825r.

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33

Nguyen, Nam T., Kristofer J. Thurecht, Steve M. Howdle, and Derek J. Irvine. "Facile one-spot synthesis of highly branched polycaprolactone." Polymer Chemistry 5, no. 8 (2014): 2997. http://dx.doi.org/10.1039/c3py01725g.

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34

Hayakawa, Yoshio, Masakazu Nishida, and Taizo Ono. "Novel polystyrene bearing highly branched hexafluoropropene trimer pendants." Polymer Bulletin 67, no. 5 (2010): 805–14. http://dx.doi.org/10.1007/s00289-010-0423-6.

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35

Li, Houbu, Litong Zhang, Laifei Cheng, Haitao Kang, and Yiguang Wang. "UV curing behavior of a highly branched polycarbosilane." Journal of Materials Science 44, no. 4 (2009): 970–75. http://dx.doi.org/10.1007/s10853-008-3216-7.

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36

Mascal, Mark, and Saikat Dutta. "Synthesis of highly-branched alkanes for renewable gasoline." Fuel Processing Technology 197 (January 2020): 106192. http://dx.doi.org/10.1016/j.fuproc.2019.106192.

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37

Bochkov, A. F., B. E. Kalganov, and V. N. Chernetskii. "Synthesis of cascadol, a highly branched functionalized polyether." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 38, no. 10 (1989): 2207. http://dx.doi.org/10.1007/bf00962157.

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38

Frey, Holger. "Highly Branched Polymers: Recent Innovations and Exciting Challenges." Macromolecular Chemistry and Physics 208, no. 15 (2007): 1613–14. http://dx.doi.org/10.1002/macp.200700344.

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39

Zaichenko, Alexander, Natalya Mitina, Kateryna Rayevska, et al. "Design of polymers of block, comb-like and highly branched structures with peroxide-containing chains." Chemistry & Chemical Technology 1, no. 2 (2007): 71–78. http://dx.doi.org/10.23939/chcht01.02.71.

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The tailored synthesis of telechelic oligoperoxides (TO), oligoperoxide metal complexes (OMC) as well as the development of controlled radical polymerization in aqueous and hydrocarbon media initiated by them provides prospective approaches for the obtaining block, comb-like and highly branched polymers with the backbone and branches of various nature, polarity, length and reactivity. The polymer-precursors and final products were investigated by chemical, spectral and rheological techniques. The novel peroxide-containing copolymers were studied in the reactions of radical polymerization in he
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40

Hood, Drew M., Ryan A. Johnson, Alex E. Carpenter, Jarod M. Younker, David J. Vinyard, and George G. Stanley. "Highly active cationic cobalt(II) hydroformylation catalysts." Science 367, no. 6477 (2020): 542–48. http://dx.doi.org/10.1126/science.aaw7742.

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The cobalt complexes HCo(CO)4 and HCo(CO)3(PR3) were the original industrial catalysts used for the hydroformylation of alkenes through reaction with hydrogen and carbon monoxide to produce aldehydes. More recent and expensive rhodium-phosphine catalysts are hundreds of times more active and operate under considerably lower pressures. Cationic cobalt(II) bisphosphine hydrido-carbonyl catalysts that are far more active than traditional neutral cobalt(I) catalysts and approach rhodium catalysts in activity are reported here. These catalysts have low linear-to-branched (L:B) regioselectivity for
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41

Chen, Wen Qiu, Chang Feng Yi, and Zu Shun Xu. "Synthesis and Characterization of Highly Branched Poly(urethane-imide)s." Advanced Materials Research 79-82 (August 2009): 1575–78. http://dx.doi.org/10.4028/www.scientific.net/amr.79-82.1575.

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A series of novel highly branched poly(urethane-imide)s (PUIs) were first successfully prep- ared by a two-step method with toluene-2,4-diisocyanate (TDI), pentaerythritol (PAT) and dianhydrides, including pyromellitic dianhydride (PMDA), 3,3′,4,4′-benzophenonetetracarboxylic dianhydride (BTDA) and 4,4'-oxydiphthalic anhydride (ODPA). It was found that the prepolymerization of PAT and TDI at 40 °C was ascertained to be 40 minutes. And the imidization of the prepolymer and PMDA was successfuly carried out after 120 °C for 2 hours. The XRD demonstrated that the obtained highly branched PUIs pre-
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42

Nguyen, Hiep, David Löf, Søren Hvilsted, and Anders Daugaard. "Highly Branched Bio-Based Unsaturated Polyesters by Enzymatic Polymerization." Polymers 8, no. 10 (2016): 363. http://dx.doi.org/10.3390/polym8100363.

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43

Nickels, Jonathan D., John Atkinson, Erzsebet Papp-Szabo, et al. "Structure and Hydration of Highly-Branched, Monodisperse Phytoglycogen Nanoparticles." Biomacromolecules 17, no. 3 (2016): 735–43. http://dx.doi.org/10.1021/acs.biomac.5b01393.

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44

Hou, Wenting, Louis Lancaster, Dongsheng Li, Ana Bowlus, Krassimir Bozhilov, and David Kisailus. "Biologically inspired synthesis of highly branched zinc oxide nanowires." Bioinspired, Biomimetic and Nanobiomaterials 3, no. 1 (2014): 10–18. http://dx.doi.org/10.1680/bbn.13.00019.

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45

Wraige, Emma J., Lesley Johns, Simon T. Belt, Guillaume Massé, Jean-Michel Robert, and Steven Rowland. "Highly branched C25 isoprenoids in axenic cultures ofHaslea ostrearia." Phytochemistry 51, no. 1 (1999): 69–73. http://dx.doi.org/10.1016/s0031-9422(98)00694-3.

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46

Świst, Agnieszka, Joanna Cabaj, Jadwiga Sołoducho, Przemysław Data, and Mieczysław Łapkowski. "Novel acridone-based branched blocks as highly fluorescent materials." Synthetic Metals 180 (September 2013): 1–8. http://dx.doi.org/10.1016/j.synthmet.2013.07.020.

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47

van der Burgt, Yuri E. M., Jack Bergsma, Ido P. Bleeker, Paul J. H. C. Mijland, Johannis P. Kamerling, and Johannes F. G. Vliegenthart. "Substituent distribution in highly branched dextrins from methylated starches." Carbohydrate Research 327, no. 4 (2000): 423–29. http://dx.doi.org/10.1016/s0008-6215(00)00062-8.

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48

Peleshanko, Sergiy, and Vladimir V. Tsukruk. "The architectures and surface behavior of highly branched molecules." Progress in Polymer Science 33, no. 5 (2008): 523–80. http://dx.doi.org/10.1016/j.progpolymsci.2008.01.003.

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49

Hong, Bo, Travis P. S. Thoms, Hunter J. Murfee, and Michael J. Lebrun. "Highly Branched Dendritic Macromolecules with Core Polyhedral Silsesquioxane Functionalities." Inorganic Chemistry 36, no. 27 (1997): 6146–47. http://dx.doi.org/10.1021/ic971034j.

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50

Robinson, Joshua W., Yan Zhou, Jun Qu, J. Timothy Bays, and Lelia Cosimbescu. "Highly branched polyethylenes as lubricant viscosity and friction modifiers." Reactive and Functional Polymers 109 (December 2016): 52–55. http://dx.doi.org/10.1016/j.reactfunctpolym.2016.10.003.

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