Results 1 to 10 of about 556,826 (407)

Lithium solvation in dimethyl sulfoxide-acetonitrile mixtures [PDF]

Journal of Chemical Physics, 2014
We present molecular dynamics simulation results pertaining to the solvation of Li+ in dimethyl sulfoxide-acetonitrile binary mixtures. The results are potentially relevant in the design of Li-air batteries that rely on aprotic mixtures as solvent media.
Calvo, Ernesto Julio, Laria, Daniel Hector, Semino, Rocio, Zaldivar, Gervasio   +3 more
core   +2 more sources

Crystal structures of polymerized lithium chloride and dimethyl sulfoxide in the form of {2LiCl·3DMSO}n and {LiCl·DMSO}n

Acta Crystallographica Section E: Crystallographic Communications, 2023
Two novel LiCl·DMSO polymer structures were created by combining dry LiCl salt with dimethyl sulfoxide (DMSO), namely, catena-poly[[chloridolithium(I)]-μ-(dimethyl sulfoxide)-κ2O:O-[chloridolithium(I)]-di-μ-(dimethyl sulfoxide)-κ4O:O], [Li2Cl2(C2H6OS)3]n,
Nichole R. Valdez, David J. Herman, Martin B. Nemer, Mark A. Rodriguez, Eric Allcorn   +4 more
doaj   +1 more source

Efficacy and safety of intravesical instillation of KRP‐116D (50% dimethyl sulfoxide solution) for interstitial cystitis/bladder pain syndrome in Japanese patients: A multicenter, randomized, double‐blind, placebo‐controlled, clinical study

International journal of urology, 2021
To evaluate the efficacy and safety of intravesical KRP‐116D, 50% dimethyl sulfoxide solution compared with placebo, in interstitial cystitis/bladder pain syndrome patients.
N. Yoshimura, Y. Homma, H. Tomoe, A. Otsuka, T. Kitta, N. Masumori, Y. Akiyama, A. Niimi, T. Mitsui, M. Nanri, T. Namima, M. Takei, A. Yamaguchi, Y. Sekiguchi, M. Kajiwara, Shinya Kobayashi, K. Ameda, Y. Ohashi, S. Sakamoto, O. Muraki, T. Shishido, S. Kageyama, K. Kokura, H. Okazoe, T. Yamanishi, Toyohiko Watanabe, T. Uno, A. Ohinata, T. Ueda   +28 more
semanticscholar   +1 more source

Dimethyl sulfoxide: a central player since the dawn of cryobiology, is efficacy balanced by toxicity?

Regenerative medicine, 2020
Dimethyl sulfoxide (DMSO) is the cryoprotectant of choice for most animal cell systems since the early history of cryopreservation. It has been used for decades in many thousands of cell transplants.
Maooz Awan, I. Buriak, R. Fleck, B. Fuller, A. Goltsev, Julie E Kerby, M. Lowdell, P. Měřička, A. Petrenko, Y. Petrenko, A. Stolzing, O. Rogulska, G. Stacey   +12 more
semanticscholar   +1 more source

Study on Autocatalytic Decomposition of Dimethyl Sulfoxide (DMSO)

Organic Process Research & Development, 2020
Dimethyl sulfoxide (DMSO) is widely used due to its excellent solvent properties; however, several serious incidents have been reported related to the use of DMSO.
Y. Deguchi, M. Kono, Yuto Koizumi, Y. Izato, A. Miyake   +4 more
semanticscholar   +1 more source

5-([(Z)-Methoxyimino]{2-[(2-methylphenoxy)methyl]phenyl}methyl)-1,3,4-oxadiazole-2(3H)-thione dimethyl sulfoxide monosolvate

IUCrData, 2023
The title compound, C18H17N3O3S·C2H6OS, crystallizes in the monoclinic space group P21/c. In the crystal, C11(9) chains of C—H...O interactions are formed, propogating in the c-axis direction.
Chetan Shrimandhar Shripanavar, Rishik Balerao, Ray J. Butcher   +2 more
doaj   +1 more source

Non-aqueous, zwitterionic solvent as an alternative for dimethyl sulfoxide in the life sciences

Communications Chemistry, 2020
Dimethyl sulfoxide (DMSO) is widely used as a solvent in the life sciences, however, it is somewhat toxic and affects cell behaviours in a range of ways.
K. Kuroda, T. Komori, Kojiro Ishibashi, Takuya Uto, Isao Kobayashi, Riki Kadokawa, Yui Kato, K. Ninomiya, Kenji Takahashi, E. Hirata   +9 more
semanticscholar   +1 more source

Vibrational spectroscopic force field studies of dimethyl sulfoxide and hexakis(dimethyl sulfoxide)scandium(III) iodide, and crystal and solution structure of the hexakis(dimethyl sulfoxide)scandium(III) ion [PDF]

, 2004
Hexakis(dimethyl sulfoxide) scandium(III) iodide, [Sc(OS(CH3)(2))(6)]I-3 contains centrosymmetric hexasolvated scandium(III) ions with an Sc-O bond distance of 2.069(3) Angstrom.
Abbasi, A., Lindqvist-Reis, P., Mink, János, Skripkin, Mikhail Yu   +3 more
core   +1 more source

(4E)-4-[(2-Hydroxyanilino)methylidene]-1-phenylpyrazolidine-3,5-dione dimethyl sulfoxide hemisolvate

Acta Crystallographica Section E, 2013
The asymmetric unit of the title compound, C16H13N3O3·0.5C2H6OS, is composed of two independent pyrazolidine-3,5-dione molecules and one dimethyl sulfoxide solvent molecule.
Mehmet Akkurt, Shaaban K. Mohamed, Mahmoud A. A. Elremaily, Eman. A. Ahmed, Mustafa R. Albayati   +4 more
doaj   +1 more source

5,5′-[1,4-Phenylenebis(methylenesulfanediyl)]bis[1,3,4-thiadiazol-2(3H)-one] dimethyl sulfoxide disolvate

Acta Crystallographica Section E, 2012
The asymmetric unit of the title compound, C12H10N4O2S4·2C2H6OS, contains one half of the p-xylene molecule and one dimethyl sulfoxide molecule. The p-xylene molecule is located about a crystallographic inversion centre.
Siyoung Jang, Sung Kwon Kang, Nam Sook Cho   +2 more
doaj   +1 more source