Diamondoids and thiadiamondoids generated from hydrothermal pyrolysis of crude oil and TSR experiments

Diamondoid compounds are widely used to reflect thermal maturation of high mature source rocks or oils and oil cracking extents. However, diamondoids and thiadiamondoids were demonstrated to have newly been generated and decomposed in our hydrothermal pyrolysis of crude oil and TSR experiments. Our results show that adamantanes and diamantanes are generated primarily within the maturity range 0.48–2.1% and 1.2–3.0% EasyRo, respectively. Their formation is enhanced and the decomposition of diamantanes obviously lags at elevated temperatures compared with anhydrous experiments. MDI, EAI, DMAI-1, DMDI-2 may serve as reliable maturity proxies at > ca.1.0% EasyRo, and other isomerization indices (TMAI-1, TMAI-2 and DMAI-2) are effective for the highly mature organic matter at EasyRo > 2.0%. The extent of oil cracking (EOC) calculated from the broadly used (3- + 4-) MD method (Dahl et al. in Nature 399:54–56, 1999) is proven to overestimate, especially for highly cracked samples due to the new generation of (3- + 4-) MD. Still, it can be corrected using a new formula at < 3.0% EasyRo. Other diamondoid-related indices (e.g., EAI, DMDI-2, As/Ds, MAs/MDs, DMAs/DMDs, and DMAs/MDs) can also be used to estimate EOC. However, these indices cannot be applied to TSR-altered petroleum. TSR is experimentally confirmed to generate diamantanes and thiaadmantanes at 1.81% EasyRo likely via direct reactions of reduced S species with hydrocarbons and accelerate the decomposition of diamantanes at > 2.62% EasyRo compared with thermal chemical alteration (TCA). More studies are needed to assess specific mechanisms for the formation of thiadiamondoids under natural conditions.

Chemical Analysis and In Vitro Bioactivity of Essential Oil of Laurelia sempervirens and Safrole Derivatives against Oomycete Fish Pathogens

In this study, the essential oil (EO) from Laurelia sempervirens was analyzed by GC/MS and safrole (1) was identified as the major metabolite 1, was subjected to direct reactions on the oxygenated groups in the aromatic ring and in the side chain, and eight compounds (4 to 12) were obtained by the process. EO and compounds 4–12 were subjected to biological assays on 24 strains of the genus Saprolegnia, specifically of the species 12 S. parasitica and 12 S. australis. EO showed a significant effect against Saprolegnia strains. Compound 6 presents the highest activity against two resistant strains, with minimum inhibitory concentration (MIC) and minimum oomyceticidal concentration (MOC) values of 25 to 100 and 75 to 125 µg/mL, respectively. The results show that compound 6 exhibited superior activities compared to the commercial controls bronopol and azoxystrobin used to combat these pathogens.

Diamondoids and Thiadiamondoids Generated From Hydrothermal Pyrolysis of Crude Oil and TSR Experiments

Diamondoid compounds are widely used to reflect thermal maturation of high mature source rocks or oils and oil cracking extents. However, diamondoids and thiadiamondoids were demonstrated to have newly been generated and decomposed in our hydrothermal pyrolysis of crude oil and TSR experiments. Our results show that adamantanes and diamantanes are generated primarily within the maturity range 0.48–2.1% and 1.2–3.0% EasyRo, respectively. Their formation is enhanced and the decomposition of diamantanes obviously lags behind at elevated temperatures compared with anhydrous experiments. MDI, EAI, DMAI-1, DMDI-2 may serve as reliable maturity proxies at > ca.1.0% EasyRo, and other isomerization indices (TMAI-1, TMAI-2 and DMAI-2) are effective for the highly mature organic matter at EasyRo > 2.0%. The extent of oil cracking (EOC) calculated from the broadly used 3-+4-MD method (Dahl et al., 1999) is proven to overestimate, especially for highly cracked samples due to the new generation of 3-+4-MD. Still, it can be corrected using a new formula at <3.0% EasyRo. Other diamondoid-related indices (e.g. EAI, DMDI-2, As/Ds, MAs/MDs, DMAs/DMDs, and DMAs/MDs) can also be used to estimate EOC. However, these indices cannot be applied to TSR-altered petroleum. TSR is experimentally confirmed to generate diamantanes and thiaadmantanes at 1.81% EasyRo via direct reactions of reduced S species with hydrocarbons and accelerate the decomposition of diamantanes at > 3.0% EasyRo compared with thermal chemical alteration (TCA).

Synthesis reactions of neutron-rich isotopes of light elements

One of the most complicated problems of experimental nuclear physics is the synthesis of exotic nuclei near the boundaries of stability. These nuclei, as a rule, are 10 or more neutrons away from stable nuclei, have a short lifetime (less than 1 ms) and low binding energy. All this determines special requirements to the choice of reactions for the synthesis of such nuclei and the method of their transportation and registration. Mainly, for the synthesis of exotic nuclei, reactions of fragmentation of the bombarding heavy ion, direct reactions of the types (p, d) , (d, p) , (d, n) , ( d , 3 He), etc., as well as reactions of fission and deep inelastic transfer are used.

A simple one-pot route to stable formamidinatoiodidolanthanoid(III) complexes from lanthanoid metals

A number of formamidinatoiodidolanthanoid(III) complexes, [Ln(DFForm)2I(thf)2] and [Ln(DFForm)I2(thf)3] (DFFormH = N,N-bis(2,6-difluorophenyl)formamidine) and [Ln(DippForm)I2(thf)3] (DippFormH = N,N-bis(2,6-diisopropylphenyl)formamidine) have been synthesized in good yields by one-pot direct reactions of the corresponding free...