Synthesis, molecular structures, and solution-phase behavior of new anionic pentacoordinate triorganotin(IV) compounds: tris(dimethylamino)sulfonium dichlorotriorganostannates, bis(2,6-dimethylphenoxy)triorganostannates, and chloro(2,6-dimethylphenoxy)triorganostannates

1990 ◽  
Vol 9 (12) ◽  
pp. 3043-3053 ◽  
Author(s):  
Masaaki Suzuki ◽  
Il Hwan Son ◽  
Ryoji Noyori ◽  
Hideki Masuda
2018 ◽  
Vol 14 (4) ◽  
pp. 305-315 ◽  
Author(s):  
Sujata D. Sakhare ◽  
V. Sai Krishna Anand ◽  
Aishwarya Karan ◽  
K. Navya Sree ◽  
S. G. Vasantharaju ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 24 (34) ◽  
pp. no-no
Author(s):  
M. G. BANWELL ◽  
M. CORBETT ◽  
J. GULBIS ◽  
M. F. MACKAY ◽  
M. E. REUM

2021 ◽  
Vol 22 (18) ◽  
pp. 9793
Author(s):  
Jain Gu ◽  
Seonggon Lee ◽  
Seunghwan Eom ◽  
Hosung Ki ◽  
Eun Hyuk Choi ◽  
...  

The halogen elimination of 1,2-diiodoethane (C2H4I2) and 1,2-diiodotetrafluoroethane (C2F4I2) serves as a model reaction for investigating the influence of fluorination on reaction dynamics and solute–solvent interactions in solution-phase reactions. While the kinetics and reaction pathways of the halogen elimination reaction of C2H4I2 were reported to vary substantially depending on the solvent, the solvent effects on the photodissociation of C2F4I2 remain to be explored, as its reaction dynamics have only been studied in methanol. Here, to investigate the solvent dependence, we conducted a time-resolved X-ray liquidography (TRXL) experiment on C2F4I2 in cyclohexane. The data revealed that (ⅰ) the solvent dependence of the photoreaction of C2F4I2 is not as strong as that observed for C2H4I2, and (ⅱ) the nongeminate recombination leading to the formation of I2 is slower in cyclohexane than in methanol. We also show that the molecular structures of the relevant species determined from the structural analysis of TRXL data provide an excellent benchmark for DFT calculations, especially for investigating the relevance of exchange-correlation functionals used for the structural optimization of haloalkanes. This study demonstrates that TRXL is a powerful technique to study solvent dependence in the solution phase.


ChemPhysChem ◽  
2019 ◽  
Vol 20 (8) ◽  
pp. 1044-1053 ◽  
Author(s):  
Santiago E. Herrera ◽  
Maximiliano L. Agazzi ◽  
M. Lorena Cortez ◽  
Waldemar A. Marmisollé ◽  
Mario Tagliazucchi ◽  
...  

2018 ◽  
Vol 51 (5) ◽  
pp. 1706-1717 ◽  
Author(s):  
Kevin Shen ◽  
Zhen-Gang Wang

Langmuir ◽  
2009 ◽  
Vol 25 (7) ◽  
pp. 3924-3931 ◽  
Author(s):  
I. Tucker ◽  
J. Penfold ◽  
R. K. Thomas ◽  
D. J. Tildesley

2017 ◽  
Vol 70 (3) ◽  
pp. 245 ◽  
Author(s):  
Sheng Liu ◽  
Chenglong Ge ◽  
Ying Ling ◽  
Haoyu Tang

Polymers with ionic liquid (IL) moieties can undergo thermally induced solution phase transitions by adjusting the balance of hydrophilicity and hydrophobicity between the cations and anions of the IL moieties, thus making them attractive candidates towards various applications such as separation, sensing, and biomedicine. In the present study, a series of poly(γ-4-methylbenzyl-l-glutamate) pyridinium tetrafluoroborate conjugates (P1–P4) containing various pyridinium moieties (i.e. pyridinium, 2-methylpyridinium, 3-methylpyridinium, and 4-methylpyridinium) were prepared by nucleophilic substitution between poly(γ-4-chloromethylbenzyl-l-glutamate) and pyridine or methylpyridines with different substituent positions, followed by ion-exchange reaction in the presence of NaBF4. 1H NMR spectroscopy and Fourier transform infrared spectroscopy analyses confirmed the molecular structures of P1–P4. 1H NMR analysis additionally revealed that P1–P4 showed high grafting efficiency in the range of 93–97 %. P1, P3, and P4 exhibited reversible UCST-type phase behaviours in both methanol and water, whereas P2 showed a reversible UCST-type phase behaviour in water only. Variable-temperature UV-visible spectroscopy was used to characterize the solution phase behaviours and UCST-type phase transition temperature (Tpt) values of P1–P4, which were in the range of 24.9–37.2°C in methanol (3 mg mL–1) and 40.9–55.7°C in water (10 mg mL–1). Tpt decreased significantly with decreasing polymer concentrations.


1998 ◽  
Vol 31 (11) ◽  
pp. 3556-3565 ◽  
Author(s):  
Ching-I Huang ◽  
Timothy P. Lodge

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