Results 71 to 80 of about 623 (115)

Pyrazinacene conjugated polymers: a breakthrough in synthesis and unraveling the conjugation continuum. [PDF]

Chem Sci
Hameed F, Maity A, Francis VS, Gavvalapalli N.   +3 more
europepmc   +1 more source

Microbial potential to mitigate neurotoxic methylmercury accumulation in farmlands and rice. [PDF]

Nat Commun
Zhou XQ, Chen KH, Yu RQ, Yang M, Liu Q, Hao YY, Li J, Liu HW, Feng J, Tan W, Huang Q, Gu B, Liu YR.   +12 more
europepmc   +1 more source

An automated high-throughput lighting system for screening photosynthetic microorganisms in plate-based formats. [PDF]

Commun Biol
Noonan AJC, Cameron PMN, Dofher K, Sukkasam N, Liu T, Rönn L, Monshupanee T, Hallam SJ.   +7 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Pentachlorophenyl organomercury compounds

Journal of Organometallic Chemistry, 1965
Abstract The following pentachlorophenyl derivatives of mercury have been prepared; (C6Cl5)2Hg, C6Cl5HgCl, C6Cl5HgCH3 and C8Cl5HgC6H5. Acid attack on the latter two species leads to scission of the C5Cl5Hg and C6H5Hg bonds respectively, in agreement with the C6F5-Hg compounds.
F.E. Paulik, S.I.E Green, R.E. Dessy
openaire   +1 more source

The mass spectra of organomercury compounds

Journal of the Chemical Society C: Organic, 1971
The fragmentation of a number of organomercury compounds under electron impact has been examined. In the symmetrical diarylmercury compounds it seems that the first fragmentation is loss of aryl radical to form arylmercury cation which then loses mercury to give aryl cation.
S W, Breuer, T E, Fear, P H, Lindsay, F G, Thorpe   +3 more
openaire   +2 more sources

Organomercury Compounds: Some Toxicological Aspects

Environmental Management and Health, 1993
Summarizes some of the most relevant toxicological aspects from the UNEP/IRPTC′s Scientific Reviews of Soviet Literature on Toxicity and Hazards of Chemicals, No. 117 Organomercury compounds, Geneva/Moscow 1990, and outlines their uses and environmental fate and pathways in a number of species and matrices.
Mervyn Richardson, I.M. Trakhtenberg, M.N. Korshun   +2 more
openaire   +1 more source

Iododemercuration of unsymmetrical organomercury compounds

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1971
1. A study was made of the kinetics of the iododemercuration of organomercury compounds, containing strong electron-acceptor substituents, in dimethylformamide and in benzene. 2. The increase in the rate of the iododemercuration reaction in the discussed series of organomercury compounds proceeds symbatically with increase in the ...
I. P. Beletskaya, L. V. Savinykh, O. A. Reutov   +2 more
openaire   +1 more source

Exchange reactions of organomercury compounds

Tetrahedron, 1975
Abstract Spectroscopic studies (PMR and UV) have been carried out on mixtures of symmetrical organomercury compounds at room temperature in DMSO, pyridine, and ethanol as solvents. It has been shown that for a range of diarylmercurials, Ar 2 Hg, and di-(acetaldehyde)mercury, Hg(CH 2 CHO) 2 , an exchange reaction occurs with the formation in solution ...
T.N. Huckerby, P.H. Lindsay, F.G. Thorpe, J.C. Podestá   +3 more
openaire   +1 more source

Organomercury Compounds in Organic Synthesis

Angewandte Chemie International Edition in English, 1978
AbstractOrganomercurials have been known since 1850 and many synthetic routes to these compounds presently exist. The ability of these compounds to accommodate a wide variety of functional groups and to tolerate quite diverse reaction conditions makes them attractive as synthetic intermediates.
openaire   +1 more source