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AbstractAbstract
[en] The authors have previously discovered that bivalent lanthanides (Ln2+) can form outer-sphere complexes of formula [LnLn](BPh4)2, where L = H2O or acetonitrile (CH3CN). The stability of the complexes decreases on going from H2O to CH3CN. This is directly correlated with the size of these solvent molecules. Clearly the larger the solvent molecule in the inner-sphere, the less stable the outer-sphere complexes. It must be mentioned that analogous complexes are not formed if the size of the solvent is further increased on going to tetrahydrofuran (THF). In aqueous-ethanol, the authors observed outer-sphere complexes with Es2+ in addition to Ln2+. The stability constants β2 varied in the order Yb2+ < Eu2+ < Es2+. Therefore, it seems interesting to determine if the order of the stability constants would change on going to organic solvents
Source
Translated from Radiokhimiya; 35: No. 5, 39-42(Sep-Oct 1993).
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Journal Article
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Translation
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AbstractAbstract
[en] The preparation of acyclic molecules featuring congested stereocenters in a 1,4-relationship in only three catalytic steps from commercially available building blocks is reported. This approach involves a diastereoselective diboration of alkenyl cyclopropyl methanol derivatives followed by a regioselective exergonic ring fragmentation. The starting materials can be prepared enantiomerically enriched and all substituents can be interconverted, therefore, this strategy allows a large variety of diversely functionalized allylboronic esters possessing distant tetrasubstituted stereocenters with high diastereoselectivity. (© 2020 Wiley‐VCH GmbH)
Primary Subject
Source
Available from: http://dx.doi.org/10.1002/anie.202010135
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Journal Article
Journal
Angewandte Chemie (International Edition); ISSN 1433-7851;
; CODEN ACIEF5; v. 59(46); p. 20434-20438

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AbstractAbstract
No abstract available
Original Title
Ustojchivost' nekotorykh karboransoderzhashchikh polimerov k dejstviyu azotnoj kisloty
Primary Subject
Source
Published in summary form only; for English translation see the journal J. Appl. Chem. USSR.
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Journal Article
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Zhurnal Prikladnoj Khimii; v. 48(7); p. 1640-1641
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AbstractAbstract
No abstract available
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Source
Vysoka Skola Chemicko-Technologicka, Prague (Czechoslovakia); p. 46; 1978; p. 46; 9th Radiochemical conference; Piestany, Czechoslovakia; 11 - 16 Sep 1978; Published in summary form only.
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Miscellaneous
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Conference
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Minaev, R.M.; Gribanova, T.N.
Eleventh international conference on boron chemistry. Programme and abstracts2002
Eleventh international conference on boron chemistry. Programme and abstracts2002
AbstractAbstract
No abstract available
Primary Subject
Source
Russian Academy of Sciences, Moscow (Russian Federation); RAS, Division of Chemistry and Material Sciences, Research Council on Organic and Organoelement Chemistry, Moscow (Russian Federation); RAS, A.N. Nesmeyanov Institute of Organoelement Compounds, Moscow (Russian Federation); RAS, N.D. Zelinsky Institute of Organic Chemistry, Moscow (Russian Federation); RAS, N.S. Kurnakov Institute of General and Inorganic Chemistry, Moscow (Russian Federation); RAS, Institute for Physical Chemistry of Ceramics, Moscow (Russian Federation); M.V. Lomonosov Moscow State University, Moscow (Russian Federation); State Scientific-Research Institute of Chemistry and Technology of Organoelement Compounds, Moscow (Russian Federation); VIAM State Research Center, Moscow (Russian Federation); 171 p; 2002; p. 50; 11. international conference on boron chemistry; Moscow (Russian Federation); 28 Jul - 2 Aug 2002
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Miscellaneous
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AbstractAbstract
No abstract available
Original Title
Sintez i nekotorye prevrashcheniya karbonil'nykh proizvodnykh 1-fenil-1,10-dikarbaklovodekaborana (10)
Primary Subject
Source
For English translation see the journal J. Gen. Chem. USSR.
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Journal Article
Journal
Zhurnal Obshchej Khimii; v. 44(1); p. 152-157
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Newman, R.N.
Central Electricity Generating Board, Berkeley (UK). Berkeley Nuclear Labs1987
Central Electricity Generating Board, Berkeley (UK). Berkeley Nuclear Labs1987
AbstractAbstract
[en] The extinguishants currently available for putting out magnesium alloy fires work by covering the burning fuel and excluding both the oxygen and nitrogen from the reaction zone. It has been reported that boron trifluoride and trimethoxi-and tributoxi-boroxine may act in a more specific chemical way on the combustion reactions. In this report an investigation into the effectiveness of these compounds on magnesium alloy fires is described. (author)
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Source
Nov 1987; 12 p
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Report
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AbstractAbstract
No abstract available
Original Title
Osnovnye zakonomernosti vosstanovitel'no-okislitel'noj izomerizatsii karboranov-12
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Source
14 refs.
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Journal Article
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Doklady Akademii Nauk SSSR; v. 231(4); p. 925-928
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AbstractAbstract
No abstract available
Original Title
Uravnenie dlya rascheta fiziko-khimicheskikh svojstv borgidridov i alkilborgidridov
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Source
Deposited article; for English translation see the journal Russ. J. Phys. Chem.
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Journal Article
Journal
Zhurnal Fizicheskoj Khimii; v. 49(6); p. 1603
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Kne, R.R.; Hawthorne, M.F.
California Univ., Oakland, CA (United States)1995
California Univ., Oakland, CA (United States)1995
AbstractAbstract
[en] A general synthetic method has been developed for the rapid and efficient production of a variety of boron-rich macromolecules suitable for conjugation with or inclusion in receptor-mediated delivery systems as well as other delivery systems. Preparation techniques have been developed to yield precisely ordered oligophosphates which are soluble, hydrophilic, may be homogeneous, and may be prepared with a variety of functional groups. (author)
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Secondary Subject
Source
5 Oct 1995; 25 Mar 1994; 60 p; WO PATENT DOCUMENT 9526359/A1/; US PATENT APPLICATION 9403272; Available from WIPO, 34, chemin des Colombettes, CH-1211 Geneva (CH); Application date: 25 Mar 1994
Record Type
Patent
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