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Journal articles on the topic 'Supra-molecular Chemistry'

To see the other types of publications on this topic, follow the link: Supra-molecular Chemistry.

Author: Grafiati

Published: 7 September 2023

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1

Chang, Yincheng, Yang Jiao, Henry E. Symons, Jiang-Fei Xu, Charl F. J. Faul, and Xi Zhang. "Molecular engineering of polymeric supra-amphiphiles." Chemical Society Reviews 48, no. 4 (2019): 989–1003. http://dx.doi.org/10.1039/c8cs00806j.

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2

Tardani, Franco, Giancarlo Masci, and Camillo La Mesa. "Block co-polymers undergoing supra-molecular association." Colloids and Surfaces A: Physicochemical and Engineering Aspects 384, no. 1-3 (July 2011): 374–80. http://dx.doi.org/10.1016/j.colsurfa.2011.04.026.

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3

Pérez, Emilio M. "Energy, supramolecular chemistry, fullerenes, and the sky." Pure and Applied Chemistry 83, no. 1 (November 12, 2010): 201–11. http://dx.doi.org/10.1351/pac-con-10-09-22.

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The search for cleaner and more abundant sources of energy is one of the major scientific challenges of the 21st century. Owing to its privileged position as the central science, chemistry is bound to play a leading role in this quest. Within the search for new materials for organic photovoltaics, some of the work we have carried out concerning the supra-molecular chemistry of electron donor and acceptor molecules is presented.

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4

Barbara, Bernard. "On the richness of supra-molecular chemistry and its openings in physics." Journal of Molecular Structure 656, no. 1-3 (August 2003): 135–40. http://dx.doi.org/10.1016/s0022-2860(03)00362-4.

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5

Singh, Suryabhan. "Silver-nitrilotriacetate coordination polymers: Supra-molecular and photoluminescence properties." Inorganica Chimica Acta 495 (September 2019): 118939. http://dx.doi.org/10.1016/j.ica.2019.05.038.

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6

Xu, XiuLing, Heng Li, Jie Xie, and JingQuan Zhao. "Molecular mechanisms for interaction of glycine betaine with supra-molecular phycobiliprotein complexes." Science in China Series B: Chemistry 52, no. 11 (November 2009): 1865–70. http://dx.doi.org/10.1007/s11426-009-0254-1.

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7

Khandelwal, Mudrika, and Alan Windle. "Origin of chiral interactions in cellulose supra-molecular microfibrils." Carbohydrate Polymers 106 (June 2014): 128–31. http://dx.doi.org/10.1016/j.carbpol.2014.01.050.

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8

Salamat, Qamar, Yadollah Yamini, Morteza Moradi, Meghdad Karimi, and Mahsa Nazraz. "Novel generation of nano-structured supramolecular solvents based on an ionic liquid as a green solvent for microextraction of some synthetic food dyes." New Journal of Chemistry 42, no. 23 (2018): 19252–59. http://dx.doi.org/10.1039/c8nj03943g.

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9

Günsel, Armağan, Ahmet T. Bilgiçli, Burak Tüzün, Hasan Pişkin, M. Nilüfer Yarasir, and Bayram Gündüz. "Optoelectronic parameters of peripherally tetra-substituted copper(ii) phthalocyanines and fabrication of a photoconductive diode for various conditions." New Journal of Chemistry 44, no. 2 (2020): 369–80. http://dx.doi.org/10.1039/c9nj05287a.

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In this study, the molecular structure of 4-(4-(trifluoromethoxy)phenoxy)phthalonitrile (1) has been elucidated and its supra-molecular dynamics have been revealed by the analysis of single crystal X-ray diffraction measurements.

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10

Chowhan, Bushra, Monika Gupta, Neha Sharma, and Antonio Frontera. "DFT analysis of supra-molecular assemblies of substituted 4H-pyran derivatives." Journal of Molecular Structure 1207 (May 2020): 127785. http://dx.doi.org/10.1016/j.molstruc.2020.127785.

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11

Jans, Anne C. H., Xavier Caumes, and Joost N. H. Reek. "Gold Catalysis in (Supra)Molecular Cages to Control Reactivity and Selectivity." ChemCatChem 11, no. 1 (October 30, 2018): 287–97. http://dx.doi.org/10.1002/cctc.201801399.

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12

Rolland-Sabaté, Agnès, Teresa Sanchez, Alain Buléon, Paul Colonna, Hernan Ceballos, Shan-Shan Zhao, Peng Zhang, and Dominique Dufour. "Molecular and supra-molecular structure of waxy starches developed from cassava (Manihot esculenta Crantz)." Carbohydrate Polymers 92, no. 2 (February 2013): 1451–62. http://dx.doi.org/10.1016/j.carbpol.2012.10.048.

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13

Groppi, Jessica, Massimo Baroncini, Margherita Venturi, Serena Silvi, and Alberto Credi. "Design of photo-activated molecular machines: highlights from the past ten years." Chemical Communications 55, no. 84 (2019): 12595–602. http://dx.doi.org/10.1039/c9cc06516d.

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14

Haw, James F., and David M. Marcus. "Well-defined (supra)molecular structures in zeolite methanol-to-olefin catalysis." Topics in Catalysis 34, no. 1-4 (May 2005): 41–48. http://dx.doi.org/10.1007/s11244-005-3798-0.

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15

Karger-Kocsis, J., and S. Keki. "Biodegradable polyester-based shape memory polymers: Concepts of (supra)molecular architecturing." Express Polymer Letters 8, no. 6 (2014): 397–412. http://dx.doi.org/10.3144/expresspolymlett.2014.44.

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16

Kitano, Hiromi, and Makoto Wakabayashi. "Pressure studies on the metallation of a supra-molecular porphyrin complex." Macromolecular Chemistry and Physics 201, no. 18 (December 1, 2000): 2775–79. http://dx.doi.org/10.1002/1521-3935(20001201)201:18<2775::aid-macp2775>3.0.co;2-7.

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17

Calabresi, Marco, Patrizia Andreozzi, and Camillo La Mesa. "Supra-molecular Association and Polymorphic Behaviour In Systems Containing Bile Acid Salts." Molecules 12, no. 8 (August 7, 2007): 1731–54. http://dx.doi.org/10.3390/12081731.

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18

Xiao, Qian, Fei Song, Wu-Cheng Nie, Xiu-Li Wang, and Yu-Zhong Wang. "Self-complementary hydrogen-bond interactions of guanosine: a hub for constructing supra-amphiphilic polymers with controlled molecular structure and aggregate morphology." Soft Matter 15, no. 1 (2019): 102–8. http://dx.doi.org/10.1039/c8sm02172d.

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A supra-amphiphilic polymer with controlled molecular structures is constructed here via self-complementary hydrogen bonding of guanosine groups between a hydrophilic poly(N-isopropylacrylamide) block and a hydrophobic poly(ε-caprolactone) block.

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19

Peckys, Diana B., Daniel Gaa, Dalia Alansary, Barbara A. Niemeyer, and Niels de Jonge. "Supra-Molecular Assemblies of ORAI1 at Rest Precede Local Accumulation into Puncta after Activation." International Journal of Molecular Sciences 22, no. 2 (January 14, 2021): 799. http://dx.doi.org/10.3390/ijms22020799.

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The Ca2+ selective channel ORAI1 and endoplasmic reticulum (ER)-resident STIM proteins form the core of the channel complex mediating store operated Ca2+ entry (SOCE). Using liquid phase electron microscopy (LPEM), the distribution of ORAI1 proteins was examined at rest and after SOCE-activation at nanoscale resolution. The analysis of over seven hundred thousand ORAI1 positions revealed a number of ORAI1 channels had formed STIM-independent distinct supra-molecular clusters. Upon SOCE activation and in the presence of STIM proteins, a fraction of ORAI1 assembled in micron-sized two-dimensional structures, such as the known puncta at the ER plasma membrane contact zones, but also in divergent structures such as strands, and ring-like shapes. Our results thus question the hypothesis that stochastically migrating single ORAI1 channels are trapped at regions containing activated STIM, and we propose instead that supra-molecular ORAI1 clusters fulfill an amplifying function for creating dense ORAI1 accumulations upon SOCE-activation.

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20

Baroncini, Massimo, Giulio Ragazzon, Serena Silvi, Margherita Venturi, and Alberto Credi. "The eternal youth of azobenzene: new photoactive molecular and supramolecular devices." Pure and Applied Chemistry 87, no. 6 (June 1, 2015): 537–45. http://dx.doi.org/10.1515/pac-2014-0903.

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AbstractThe development of multicomponent chemical systems that can perform predetermined functions under external control – i.e., molecular devices – is a challenging task in chemistry and a fascinating objective in the frame of a bottom-up approach to nanostructures. Photochromic units undergo profound changes in their chemical and/or electronic structure upon light excitation, and are highly interesting for the construction of photocontrollable molecular devices, machines and materials. The E–Z photoisomerization of azobenzene – owing to its high efficiency, excellent reversibility and significant physico-chemical differences between the two forms – is a highly useful reaction in this regard. Azobenzene photoisomerization has been known for almost 80 years and has been exploited to implement light-induced functionalities with a large variety of compounds, biomolecules, nanosystems and materials. Here we present some of our recent investigations highlighting how this outstanding photochrome can be utilized to develop (supra)molecular systems with valuable light-induced functionalities.

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21

Wei, Shenghui, Weiheng Huang, Fengmei Su, Xiaoliang Tang, Ningdong Huang, and Liangbin Li. "Lyotropic meso-phase behavior of supra-molecular nanotubes with helical charge distribution." Soft Matter 13, no. 19 (2017): 3475–79. http://dx.doi.org/10.1039/c7sm00603a.

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22

Balzani, Vincenzo, Paola Ceroni, and Belén Ferrer. "Molecular devices." Pure and Applied Chemistry 76, no. 10 (January 1, 2004): 1887–902. http://dx.doi.org/10.1351/pac200476101887.

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The concept of a macroscopic device can be extended to the molecular level by designing and synthesizing (supra)molecular species capable of performing specific functions. Molecular devices need energy to operate and signals to communicate with the operator. The energy needed to make a device work can be supplied as chemical energy, electrical energy, or light. Luminescence is one of the most useful techniques to monitor the operation of molecular-level devices. The extension of the concept of a device to the molecular level is of interest, not only for basic research, but also for the growth of nanoscience and the development of nanotechnology. In this article, some of the most recent experiments performed in our laboratory will be reviewed.

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23

Wang, Zi-Liang, Lin-Heng Wei, Ming-Xue Li, and Jing-Ping Wang. "Synthesis, crystal structure and theoretical investigation of two infinite two-dimensional supra-molecular compounds." Journal of Molecular Structure 879, no. 1-3 (May 2008): 150–55. http://dx.doi.org/10.1016/j.molstruc.2007.08.025.

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24

Bowen, Phillip, and Norman L. Allinger. "Molecular mechanics studies on the supra annular effect of 3-cyclohexene-1-carboxaldehyde compounds." Journal of Organic Chemistry 51, no. 9 (May 1986): 1513–16. http://dx.doi.org/10.1021/jo00359a024.

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25

Hadnađev, Miroslav, Tamara Dapčević‐Hadnađev, Ivana Pajić‐Lijaković, Jasna Mastilović, and Branko Bugarski. "Molecular and Supra‐Molecular Structural Ordering of Wheat Starch‐OSA Modified Waxy Maize Starch Mixtures During Storage." Starch - Stärke 71, no. 9-10 (May 31, 2019): 1800225. http://dx.doi.org/10.1002/star.201800225.

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26

Bedford, S. E., T. M. Nicholson, and A. H. Windle. "A supra-molecular approach to the modelling of textures in liquid crystals." Liquid Crystals 10, no. 1 (July 1991): 63–71. http://dx.doi.org/10.1080/02678299108028229.

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27

Demers, Jean-Philippe, Pascal Fricke, Chaowei Shi, Veniamin Chevelkov, and Adam Lange. "Structure determination of supra-molecular assemblies by solid-state NMR: Practical considerations." Progress in Nuclear Magnetic Resonance Spectroscopy 109 (December 2018): 51–78. http://dx.doi.org/10.1016/j.pnmrs.2018.06.002.

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28

Shen, Hong, Kwang-Un Jeong, Huiming Xiong, Matthew J. Graham, Siwei Leng, Joseph X. Zheng, Huabing Huang, Mingming Guo, Frank W. Harris, and Stephen Z. D. Cheng. "Phase behaviors and supra-molecular structures of a series of symmetrically tapered bisamides." Soft Matter 2, no. 3 (2006): 232. http://dx.doi.org/10.1039/b516557a.

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29

Yu, Guocan, Jie Yang, Danyu Xia, and Yong Yao. "An enzyme-responsive supra-amphiphile constructed by pillar[5]arene/acetylcholine molecular recognition." RSC Adv. 4, no. 36 (2014): 18763–71. http://dx.doi.org/10.1039/c4ra01820f.

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30

Li, Gui-an, Xiu Li, Jian-ping Song, Fa-rong Li, Shao-hua Ma, Yu-rong Zhang, and Xiao-ling Fang. "Preparation and Fluorescence Properties of Co-doped Nanocomposite Film Based on Supra Molecular Structure." Chinese Journal of Chemical Physics 19, no. 2 (August 2006): 183–86. http://dx.doi.org/10.1360/cjcp2006.19(2).183.4.

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31

Kumar, A. V. N. Ashok, M. Muniprasad, A. V. S. N. Krishna Murthy, P. V. Chalapathi, and D. M. Potukuchi. "Relaxation behavior of supra-molecular hydrogen-bonded liquid crystal phase structures: SA:11OBA." Molecular Crystals and Liquid Crystals 624, no. 1 (January 2, 2016): 28–43. http://dx.doi.org/10.1080/15421406.2015.1038884.

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32

Zhou, Xiao-He, Yu Fan, Wan-Xia Li, Xiang Zhang, Rong-Ran Liang, Feng Lin, Tian-Guang Zhan, et al. "Viologen derivatives with extended π-conjugation structures: From supra-/molecular building blocks to organic porous materials." Chinese Chemical Letters 31, no. 7 (July 2020): 1757–67. http://dx.doi.org/10.1016/j.cclet.2019.12.039.

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33

XIANG, Jun-Feng, Ping-Gui YI, Zhi-Yong REN, Xian-Yong YU, Jian CHEN, Wu LIU, and Tao-Mei LI. "Effect of Supra-Molecular Interaction on the Intramolecular Proton Transfer of 2-(2-Aminophenyl)benzothiazole." Acta Physico-Chimica Sinica 32, no. 3 (2016): 624–30. http://dx.doi.org/10.3866/pku.whxb201512291.

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34

Zhang, Jing, and Long-Guan Zhu. "Syntheses, structures, and supra-molecular assembles of zinc 4-sulfobenzoate complexes with chelating and/or bridging ligands." Journal of Molecular Structure 931, no. 1-3 (August 2009): 87–93. http://dx.doi.org/10.1016/j.molstruc.2009.05.032.

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35

Prabu, N. Pongali Sathya, and M. L. N. Madhu Mohan. "Optical Shuttering and Filtering Action in Nematogens of Supra Molecular Hydrogen-Bonded Liquid Crystals." Molecular Crystals and Liquid Crystals 557, no. 1 (March 20, 2012): 190–205. http://dx.doi.org/10.1080/15421406.2011.648059.

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36

Tan, Hueyling. "Factors Affecting Molecular Self-Assembly and Its Mechanism." Scientific Research Journal 9, no. 1 (June 30, 2012): 43. http://dx.doi.org/10.24191/srj.v9i1.5385.

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Molecular self-assembly is ubiquitous in nature and has emerged as a new approach to produce new materials in chemistry, engineering, nanotechnology, polymer science and materials. Molecular self-assembly has been attracting increasing interest from the scientific community in recent years due to its importance in understanding biology and a variety of diseases at the molecular level. In the last few years, considerable advances have been made in the use ofpeptides as building blocks to produce biological materials for wide range of applications, including fabricating novel supra-molecular structures and scaffolding for tissue repair. The study ofbiological self-assembly systems represents a significant advancement in molecular engineering and is a rapidly growing scientific and engineering field that crosses the boundaries ofexisting disciplines. Many self-assembling systems are rangefrom bi- andtri-block copolymers to DNA structures as well as simple and complex proteins andpeptides. The ultimate goal is to harness molecular self-assembly such that design andcontrol ofbottom-up processes is achieved thereby enabling exploitation of structures developed at the meso- and macro-scopic scale for the purposes oflife and non-life science applications. Such aspirations can be achievedthrough understanding thefundamental principles behind the selforganisation and self-synthesis processes exhibited by biological systems.

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37

Tan, Huey Ling. "Factors Affecting Molecular Self-Assembly and Its Mechanism." Scientific Research Journal 9, no. 1 (June 1, 2012): 43. http://dx.doi.org/10.24191/srj.v9i1.9414.

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Molecular self-assembly is ubiquitous in nature and has emerged as a new approach to produce new materials in chemistry, engineering, nanotechnology, polymer science and materials. Molecular self-assembly has been attracting increasing interest from the scientific community in recent years due to its importance in understanding biology and a variety of diseases at the molecular level. In the last few years, considerable advances have been made in the use of peptides as building blocks to produce biological materials for wide range of applications, including fabricating novel supra-molecular structures and scaffolding for tissue repair. The study of biological self-assembly systems represents a significant advancement in molecular engineering and is a rapidly growing scientific and engineering field that crosses the boundaries of existing disciplines. Many self-assembling systems are range from bi- and tri-block copolymers to DNA structures as well as simple and complex proteins and peptides. The ultimate goal is to harness molecular self-assembly such that design and control of bottom-up processes is achieved thereby enabling exploitation of structures developed at the meso- and macro-scopic scale for the purposes of life and non-life science applications. Such aspirations can be achieved through understanding the fundamental principles behind the self organisation and self-synthesis processes exhibited by biological systems.

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38

Gangu, Kranthi Kumar, Suresh Maddila, Saratchandra Babu Mukkamala, and Sreekantha B. Jonnalagadda. "Catalytic activity of supra molecular self-assembled Nickel (II) coordination complex in synthesis of indeno-pyrimidine derivatives." Polyhedron 158 (January 2019): 464–70. http://dx.doi.org/10.1016/j.poly.2018.11.041.

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39

Ghosh, Amit, Indrajit Paul, and Michael Schmittel. "Time-Dependent Pulses of Lithium Ions in Cascaded Signaling and Out-of-Equilibrium (Supra)molecular Logic." Journal of the American Chemical Society 141, no. 48 (November 18, 2019): 18954–57. http://dx.doi.org/10.1021/jacs.9b10763.

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40

Privalov, Peter L. "Thermodynamic problems in structural molecular biology." Pure and Applied Chemistry 79, no. 8 (January 1, 2007): 1445–62. http://dx.doi.org/10.1351/pac200779081445.

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The most essential feature of living biological systems is their high degree of structural organization. The key role is played by two linear heteropolymers, the proteins and nucleic acids. Under environmental conditions close to physiological, these biopolymers are folded into unique native conformations, genetically determined by the arrangement of their standard building blocks. In their native conformation, biological macromolecules recognize their partners and associate with them, forming specific, higher-order complexes, the "molecular machines". Folding of biopolymers into their native conformation and their association with partners is in principle a reversible, thermodynamically driven process. Investigation of the thermodynamics of these basic biological processes has prime importance for understanding the mechanisms of forming these supra-macromolecular constructions and their functioning.

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41

Shen, Yanting, Xue Zhang, Lijia Liang, Jing Yue, Dianshuai Huang, Weiqing Xu, Wei Shi, Chongyang Liang, and Shuping Xu. "Mitochondria-targeting supra-carbon dots: Enhanced photothermal therapy selective to cancer cells and their hyperthermia molecular actions." Carbon 156 (January 2020): 558–67. http://dx.doi.org/10.1016/j.carbon.2019.09.079.

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42

Bucknall, Clive, Volker Altstädt, Dietmar Auhl, Paul Buckley, Dirk Dijkstra, Andrzej Galeski, Christoph Gögelein, et al. "Structure, processing and performance of ultra-high molecular weight polyethylene (IUPAC Technical Report). Part 2: crystallinity and supra molecular structure." Pure and Applied Chemistry 92, no. 9 (August 25, 2020): 1485–501. http://dx.doi.org/10.1515/pac-2019-0403.

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AbstractTest methods including OM, SEM, TEM, DSC, SAXS, WAXS, and IR were used to characterise supra-molecular structure in three batches of polyethylene (PE), which had weight-average relative molar masses ${\overline{M}}_{\text{w}}$of approximately 0.6 × 106, 5 × 106, and 9 × 106. They were applied to compression mouldings made by the polymer manufacturer. Electron microscopy showed that powders formed in the polymerization reactor consisted of irregularly shaped grains between 50 and 250 μm in diameter. Higher magnification revealed that each grain was an aggregate, composed of particles between 0.4 and 0.8 μm in diameter, which were connected by long, thin fibrils. In compression mouldings, lamellar thicknesses ranged from 7 to 23 nm. Crystallinity varied between 70 and 75 % in reactor powder, but was lower in compression mouldings. Melting peak temperatures ranged from 138 to 145 °C, depending on processing history. DMTA showed that the glass transition temperature θg was −120 °C for all three grades of polyethylene. IR spectroscopy found negligibly small levels of oxidation and thermal degradation in mouldings. Optical microscopy revealed the presence of visible fusion defects at grain boundaries. It is concluded that relatively weak defects can be characterized using optical microscopy, but there is a need for improved methods that can detect less obvious fusion defects.

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43

Lu, Xiaoming, Bo Liu, Shuo Wang, and Yuan Deng. "Self-assembly of chiral porous supra-molecular complex with three-dimensional nano-cage structure filled with guest molecule." Inorganic Chemistry Communications 9, no. 4 (April 2006): 403–6. http://dx.doi.org/10.1016/j.inoche.2006.01.008.

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44

Velyvis, Algirdas, Howard K. Schachman, and Lewis E. Kay. "Assignment of Ile, Leu, and Val Methyl Correlations in Supra-Molecular Systems: An Application to Aspartate Transcarbamoylase." Journal of the American Chemical Society 131, no. 45 (November 18, 2009): 16534–43. http://dx.doi.org/10.1021/ja906978r.

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45

Milovanovic, Branislav, Milena Petkovic, and Mihajlo Etinski. "Properties of the excited electronic states of guanine quartet complexes with alkali metal cations." Journal of the Serbian Chemical Society 85, no. 8 (2020): 1021–32. http://dx.doi.org/10.2298/jsc191025140m.

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G-quartets are supra-molecular structures that consist of four guanine molecules connected by eight hydrogen bonds. They are additionally stabilized by metal cations. In this contribution, the excited states of G-quartet and its complexes with lithium, sodium and potassium were studied by employing time-dependent density functional theory. The findings indicate that vertical excitations from the optimized ground state involve transitions from several bases, whereas excitations from the optimized lowest excited state include transitions from one base. The charge-transfer character of these states was analyzed. It was shown that the cations are able to modify positions of the maxima of the fluorescence spectra of the complexes.

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46

Martí-Centelles, Rosa, Jenifer Rubio-Magnieto, and Beatriu Escuder. "A minimalistic catalytically-active cell mimetic made of a supra-molecular hydrogel encapsulated into a polymersome." Chemical Communications 56, no. 92 (2020): 14487–90. http://dx.doi.org/10.1039/d0cc04941g.

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47

Farooq, Muhammad Awais, Wei Ma, Shuxing Shen, and Aixia Gu. "Underlying Biochemical and Molecular Mechanisms for Seed Germination." International Journal of Molecular Sciences 23, no. 15 (July 31, 2022): 8502. http://dx.doi.org/10.3390/ijms23158502.

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With the burgeoning population of the world, the successful germination of seeds to achieve maximum crop production is very important. Seed germination is a precise balance of phytohormones, light, and temperature that induces endosperm decay. Abscisic acid and gibberellins—mainly with auxins, ethylene, and jasmonic and salicylic acid through interdependent molecular pathways—lead to the rupture of the seed testa, after which the radicle protrudes out and the endosperm provides nutrients according to its growing energy demand. The incident light wavelength and low and supra-optimal temperature modulates phytohormone signaling pathways that induce the synthesis of ROS, which results in the maintenance of seed dormancy and germination. In this review, we have summarized in detail the biochemical and molecular processes occurring in the seed that lead to the germination of the seed. Moreover, an accurate explanation in chronological order of how phytohormones inside the seed act in accordance with the temperature and light signals from outside to degenerate the seed testa for the thriving seed’s germination has also been discussed.

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48

Banjare, Manoj Kumar, Kamalakanta Behera, Manmohan L. Satnami, Siddharth Pandey, and Kallol K. Ghosh. "Supra-molecular inclusion complexation of ionic liquid 1-butyl-3-methylimidazolium octylsulphate with α- and β-cyclodextrins." Chemical Physics Letters 689 (December 2017): 30–40. http://dx.doi.org/10.1016/j.cplett.2017.09.033.

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49

Yan, Li, Chuanbi Li, and Xiaoli Chen. "Hydrogen bonded supra-molecular framework in inorganic–organic hybrid compounds of Mn(II) and Zn(II): Syntheses, structures, and photoluminescent studies." Journal of Molecular Structure 1058 (January 2014): 277–83. http://dx.doi.org/10.1016/j.molstruc.2013.11.026.

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50

Stoiljkovic, Dragoslav, Budimir Damjanovic, Jovica Djordjevic, Danko Spehar, and Slobodan Jovanovic. "Compressed ethylene phase states and their importance for the production of low density polyethylene." Chemical Industry 60, no. 11-12 (2006): 283–86. http://dx.doi.org/10.2298/hemind0612283s.

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In the last three decades the authors have published papers on the concept of the supra-molecular organization and the phase state of compressed ethylene gas and their effects on the mechanism and kinetics of free-radical ethylene polymerization. The effects on the macromolecular structure of low density polyethylene (LDPE) were also explained. The importance of the phase state of compressed ethylene on the industrial process of LDPE production are presented in this paper: The start-up of polymerization, the peak in the polymerization rate curve, the stability of the reaction, the structure and properties of LDPE, the separation of unreacted ethylene and polyethylene and ethylene compression are discussed.

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