Stereoselective Primary and Secondary Nucleation Events in Multicomponent Seeded Supramolecular Polymerization

2021 ◽  
Author(s):  
Souvik Sarkar ◽  
Aritra Sarkar ◽  
Arka Som ◽  
Sarit S. Agasti ◽  
Subi J. George
Keyword(s):  
Secondary Nucleation ◽  
Supramolecular Polymerization

Continuous Precipitation of Lead Iodide

1994 ◽  
Vol 59 (7) ◽  
pp. 1503-1510
Author(s):  
Stanislav Žáček ◽  
Jaroslav Nývlt
Keyword(s):  
Growth Rate ◽  
Particle Size ◽  
Crystal Size ◽  
Crystal Growth Rate ◽  
Laboratory Model ◽  
Lead Iodide ◽  
Secondary Nucleation ◽  
Equimolar Ratio ◽  
Continuous Precipitation ◽  
The Mean

Lead iodide was precipitated from aqueous solutions of 0.015 - 0.1 M Pb(NO3)2 and 0.03 - 0.2 M KI in the equimolar ratio using a laboratory model of a stirred continuous crystallizer at 22 °C. After reaching the steady state, the PbI2 crystal size distribution was measured sedimentometrically and the crystallization kinetics was evaluated based on the mean particle size. Both the linear crystal growth rate and the nucleation rate depend on the specific output of the crystallizer. The system crystallization constant either points to a significant effect of secondary nucleation by the mechanism of contact of the crystals with the stirrer blade, or depends on the concentrations of the components added due to the micromixing mechanism.

Batch Crystallization with Crystals Attrition

1993 ◽  
Vol 58 (8) ◽  
pp. 1855-1860 ◽  
Author(s):  
Jaroslav Nývlt ◽  
Stanislav Žáček
Keyword(s):  
Mathematical Model ◽  
Calcium Sulfate ◽  
Crystal Size ◽  
Theoretical Description ◽  
Secondary Nucleation ◽  
Batch Crystallization ◽  
Batch Time ◽  
The Mean

The dependence of the mean crystal size of the products from batch crystallizers on the batch time occasionally exhibits a maximum, which can be explained by secondary nucleation due to the attrition of crystals. A kinetic equatation of nucleation, comprising a term for crystal attrition, can be used for the theoretical description of such behaviour. A mathematical model of a batch crystallizer with crystal attrition has been verified on the calcium sulfate precipitation.

Directional Supramolecular Polymerization in a Dynamic Microsolution: A Linearly Moving Polymer’s End Striking Monomers

2021 ◽  
Author(s):  
Shota Matoba ◽  
Chisako Kanzaki ◽  
Kae Yamashita ◽  
Takahiro Kusukawa ◽  
Gaku Fukuhara ◽  
...  
Keyword(s):  
Supramolecular Polymerization

scholarly journals Oriented arrangement of simple monomers enabled by confinement: towards living supramolecular polymerization

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yingtong Zong ◽  
Si-Min Xu ◽  
Wenying Shi ◽  
Chao Lu
Keyword(s):  
Activation Barrier ◽  
Degree Of Polymerization ◽  
Supramolecular Polymer ◽  
Energy Principle ◽  
Spontaneous Nucleation ◽  
Pyrene Derivatives ◽  
Multifunctional Molecules ◽  
Double Hydroxide ◽  
Supramolecular Polymerization ◽  
Kinetics Of

AbstractThe living supramolecular polymerization technique provides an exciting research avenue. However, in comparison with the thermodynamic spontaneous nucleation, using simple monomers to realize living supramolecular polymerization is hardly possible from an energy principle. This is because the activation barrier of kinetically trapped simple monomer (nucleation step) is insufficiently high to control the kinetics of subsequent elongation. Here, with the benefit of the confinement from the layered double hydroxide (LDH) nanomaterial, various simple monomers, (such as benzene, naphthalene and pyrene derivatives) successfully form living supramolecular polymer (LSP) with length control and narrow dispersity. The degree of polymerization can reach ~6000. Kinetics studies reveal LDH overcomes a huge energy barrier to inhibit undesired spontaneous nucleation of monomers and disassembly of metastable states. The universality of this strategy will usher exploration into other multifunctional molecules and promote the development of functional LSP.

scholarly journals Supramolecular Systems Containing B–N Frustrated Lewis Pairs of Tris(pentafluorophenyl)borane and Triphenylamine Derivatives

2021 ◽  
Vol 03 (02) ◽  
pp. 174-183
Author(s):  
P. Chidchob ◽  
S. A. H. Jansen ◽  
S. C. J. Meskers ◽  
E. Weyandt ◽  
N. P. van Leest ◽  
...  
Keyword(s):  
Materials Science ◽  
Supramolecular Polymers ◽  
Frustrated Lewis Pairs ◽  
Paramagnetic Resonance ◽  
Donor And Acceptor ◽  
Donor Acceptor ◽  
Noncovalent Polymers ◽  
Electron Paramagnetic ◽  
Supramolecular Polymerization ◽  
Lewis Pairs

The introduction of a chemical additive to supramolecular polymers holds high potential in the development of new structures and functions. In this regard, various donor- and acceptor-based molecules have been applied in the design of these noncovalent polymers. However, the incorporation of boron–nitrogen frustrated Lewis pairs in such architectures is still rare despite their many intriguing properties in catalysis and materials science. The limited choices of suitable boron derivatives represent one of the main limitations for the advancement in this direction. Here, we examine the use of the commercially available tris(pentafluorophenyl)borane with various triphenylamine derivatives to create supramolecular B–N charge transfer systems. Our results highlight the importance of a proper balance between the donor/acceptor strength and the driving force for supramolecular polymerization to achieve stable, long-range ordered B–N systems. Detailed analyses using electron paramagnetic resonance and optical spectroscopy suggest that tris(pentafluorophenyl)borane displays complex behavior with the amide-based triphenylamine supramolecular polymers and may interact in dimers or larger chiral aggregates, depending on the specific structure of the triphenylamines.

Supramolecular Polymerization‐Induced Nanoassemblies for Self‐Augmented Cascade Chemotherapy and Chemodynamic Therapy of Tumour

2021 ◽  
Author(s):  
Kuikun Yang ◽  
Zhiqing Yang ◽  
Ludan Yue ◽  
Guocan Yu ◽  
Xiangjun Zhang ◽  
...  
Keyword(s):  
Supramolecular Polymerization

scholarly journals Living supramolecular polymerization of fluorinated cyclohexanes

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Oleksandr Shyshov ◽  
Shyamkumar Vadakket Haridas ◽  
Luca Pesce ◽  
Haoyuan Qi ◽  
Andrea Gardin ◽  
...  
Keyword(s):  
Dipole Moment ◽  
Self Assembly ◽  
Materials Science ◽  
Helical Structure ◽  
The Self ◽  
Supramolecular Polymers ◽  
Aliphatic Compound ◽  
Double Helical Structure ◽  
Key Driver ◽  
Supramolecular Polymerization

AbstractThe development of powerful methods for living covalent polymerization has been a key driver of progress in organic materials science. While there have been remarkable reports on living supramolecular polymerization recently, the scope of monomers is still narrow and a simple solution to the problem is elusive. Here we report a minimalistic molecular platform for living supramolecular polymerization that is based on the unique structure of all-cis 1,2,3,4,5,6-hexafluorocyclohexane, the most polar aliphatic compound reported to date. We use this large dipole moment (6.2 Debye) not only to thermodynamically drive the self-assembly of supramolecular polymers, but also to generate kinetically trapped monomeric states. Upon addition of well-defined seeds, we observed that the dormant monomers engage in a kinetically controlled supramolecular polymerization. The obtained nanofibers have an unusual double helical structure and their length can be controlled by the ratio between seeds and monomers. The successful preparation of supramolecular block copolymers demonstrates the versatility of the approach.

Counteranion- and Solvent-Mediated Chirality Transfer in the Supramolecular Polymerization of Luminescent Platinum(II) Complexes

2018 ◽  
Vol 57 (52) ◽  
pp. 17189-17193 ◽  
Author(s):  
Qingyun Wan ◽  
Xin-Shan Xiao ◽  
Wai-Pong To ◽  
Wei Lu ◽  
Yong Chen ◽  
...  
Keyword(s):  
Chirality Transfer ◽  
Supramolecular Polymerization
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