نتایج جستجو برای: ion pair complex formation

تعداد نتایج: 1528000  

Journal: :international journal of nano dimension 0
a. phuruangrat department of materials science and technology, faculty of science,prince of songkla university, hat yai, songkhla 90112, thailand. t. thongtem department of chemistry, faculty of science, chiang mai university,chiang mai 50200, thailand. s. thongtem department of physics and materials science, faculty of science, chiang mai university, chiang mai 50200, thailand.

lini0.5co0.5vo4 has been successfully synthesized by tartate precursor combustion method using li2co3, co(no3)2.6h2o, ni(no3)2.6h2o and nh4vo3 as a starting materials in deionized water with the subsequent calcination at 450-600 oc for 12 h. the combustion and decomposition of tartate precursor were studied by tga and compared with tartaric acid. it found weight loss at 50-450 oc. the product s...

Journal: :Dalton transactions 2009
Roberta Bomparola Robert P Davies Stefan Hornauer Andrew J P White

The organo-amidocuprate [Cu(2)Li(2)Mes(2)(N(CH(2)Ph)(2))(2)] is solvated by thf to yield the monomeric contact ion pair complex [MesCuN(CH(2)Ph)(2).Li(thf)(3)] in which the Li cation is bound to the amido nitrogen; this behaviour differs significantly from that observed in diorganocuprates which favour solvent separate ion pairs.

Journal: :Chemistry 2017
Soham Mandal Marian Hebenbrock Jens Müller

1,N6 -Ethenoadenine (ϵA) and cytosine (C) are able to form two different metal-mediated base pairs. When the glycosidic bonds are arranged in a cisoid manner (i.e., in antiparallel-stranded DNA), the ϵA:C mispair binds one AgI ion, leading to a mononuclear ϵA-AgI -C base pair that contains a synergistic hydrogen bond. In contrast, a transoid orientation of the glycosidic bonds (as found in para...

Journal: :The Journal of the Society of Chemical Industry, Japan 1971

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