Zobrazeno 1 - 10
of 56
pro vyhledávání: '"dimethylaluminum chloride"'
Autor:
Mutasem Z. Bani-Fwaz
Publikováno v:
Inorganic and Nano-Metal Chemistry. 50:956-963
The reaction of tris(trimethylsilyl)phosphine with dimethylaluminum chloride in 1,2-dimethoxyethane (monoglyme) displays an important role as building blocks that results in the production of novel...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9ce983b94d329c663662aab4771fe18
https://doi.org/10.1080/24701556.2020.1729192
https://doi.org/10.1080/24701556.2020.1729192
Autor:
Younghee Lee, Steven M. George
Publikováno v:
The Journal of Physical Chemistry C. 123:18455-18466
Atomic layer etching (ALE) of Al2O3, HfO2, and ZrO2 was accomplished using sequential exposures with hydrogen fluoride (HF) as the fluorination reagent and dimethylaluminum chloride (DMAC, AlCl(CH3...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::804ea904e22e991b6f53ff1bcbd4bcf8
https://doi.org/10.1021/acs.jpcc.9b04767
https://doi.org/10.1021/acs.jpcc.9b04767
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 125:110-113
A gasometric titration method was developed to quantitate active alkylaluminum content in dimethylaluminum chloride solution to perform the stoichiometry calculation for the reaction charge. The procedure was reproducible with good precision, and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4d7d6e33305f80ccf49ac6ca1bdccc9
https://doi.org/10.1016/j.jpba.2016.03.022
https://doi.org/10.1016/j.jpba.2016.03.022
Akademický článek
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Publikováno v:
Organic letters. 19(9)
A general and efficient method for the synthesis of pronucleotide (ProTide) 5'-phosphoramidate monoesters is reported. This method consists of a highly stereoselective 5'-phosphorylation mediated by dimethylaluminum chloride to afford the desired tar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6af197adcb55bed1fadb8c6e80ac75c
https://pubmed.ncbi.nlm.nih.gov/28418681
https://pubmed.ncbi.nlm.nih.gov/28418681
Publikováno v:
Advanced Electronic Materials. 3(6)
Dimethylaluminum chloride (DMACl) as an aluminum source has shown promising potential to replace more expensive and commonly used trimethylaluminum in the semiconductor industry for atomic layer deposited (ALD) thin films. Here, the Al2O3 DMACl-proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6728dded88f041d27953e5c7e37dfd36
https://doi.org/10.1002/aelm.201600491
https://doi.org/10.1002/aelm.201600491
Dimethylaluminum chloride (DMACl) as an aluminum source has shown promising potential to replace more expensive and commonly used trimethylaluminum in the semiconductor industry for atomic layer deposited (ALD) thin films. Here, the Al2O3 DMACl-proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1222::fd43ba42a65f2f7bd55aa7f2eba02776
http://urn.fi/URN:NBN:fi:jyu-201711294421
http://urn.fi/URN:NBN:fi:jyu-201711294421
Dimethylaluminum chloride (DMACl) is a cost-effective aluminium precursor alternative to conventional trimethylaluminium (TMA) for Atomic Layer Deposited (ALD) Al 2 O 3. The DMACl water process shows better passivation after high temperature firing w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b70bada9f68597349e6f3eea4b9a582f
https://aaltodoc.aalto.fi/handle/123456789/24859
https://aaltodoc.aalto.fi/handle/123456789/24859
Publikováno v:
Angewandte Chemie International Edition. 50:12067-12070
The use of organoaluminum compounds in catalytic or stoichiometric amounts is crucial for the success.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b30752e3a92c52efe22ab787b21601f
https://doi.org/10.1002/anie.201106174
https://doi.org/10.1002/anie.201106174
Publikováno v:
Inorganic Chemistry. 50:7838-7845
Reaction of [V(X)(OR)(3)] (X = O, Np-tolyl, R = nPr, tBu) with 5,11,17,23-tBu-25,27-dihydroxycalix[4]arene (LH(2)) led to the formation of [V(X)(OR)L](2) X = O, R = nPr (1); X = Np-tolyl, R = nPr (2); X = Np-tolyl, R = tBu (3) as the major product. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1ac4efb4d7d69ce89aa58ef270c11ab
https://doi.org/10.1021/ic2010198
https://doi.org/10.1021/ic2010198