Vram Dovlatyan

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Vram Dovlatyan
Վռամ Դովլաթյան
Dovlatyan-Vram.jpg
Born(1923-07-13)13 July 1923
Died25 December 2005(2005-12-25) (aged 82)
Nationality Armenian
Citizenship Soviet, Armenia
Alma mater Yerevan State University
Awards Order of the Patriotic War (1985)
Order of the Red Banner of Labour (2)
Order of the Badge of Honour
Scientific career
Fieldschemical
Institutions Armenian National Agrarian University

Vram Vaginaki Dovlatyan (August 13, 1923, Nor Bayazet - December 25, 2005, Yerevan) was a Soviet and Armenian organic chemist, Doctor of Chemical Sciences (1965), professor (1967), and Honored Scientist of the Armenian SSR (1980). He was also an Academician of the Academy of Sciences of the Armenian SSR (1994, corresponding member 1986). [1] He is the elder brother of Frunze Dovlatyan.

Contents

Biography

Vram Dovlatyan was born in Nor Bayazet. He participated in the Great Patriotic War and worked there as a coder at the headquarters. In 1949 he graduated from the Faculty of Chemistry of Yerevan State University.

Since 1954, he worked at the Department of General Chemistry of the Armenian Agricultural Institute, from 1958 to 1989 he served as head of the Department of General Chemistry.

From 1962 to 2005, he was the head of the Laboratory of Pesticide Problems at the same institute, and since 1962 he also headed the experimental laboratory for the synthesis of pesticides. Full member of the RAS since 1994. [1]

New highly active herbicides, fungicides and growth stimulants discovered in the Dovlatyanovsky scientific laboratory are widely used in agriculture. He studied the reactions of chloromethoxymethylation of the ester acetic acid, the catalytic effect of quaternary ammonium salts on the formation of esters carbonic acid. Unique rearrangement reactions of chloralkox (thio, amine-sim-triazines) were discovered (in combination with the production of tara-sim-triazines). [2]

Works

Author of about 450 scientific works, including 130 copyright certificates. Based on his developments, 4 doctoral and 50 candidate dissertations were defended.

For 40 years he headed the department of general chemistry of the Armenian Agricultural Institute, now the State Agrarian University of Armenia. There he created a problematic laboratory for the synthesis and testing of pesticides, which he led until the end of his life. [2]

Awards

Related Research Articles

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Herbicides, also commonly known as weed killers, are substances used to control undesired plants, also known as weeds. Selective herbicides control specific weed species while leaving the desired crop relatively unharmed, while non-selective herbicides kill plants indiscriminately. The combined effects of herbicides, nitrogen fertilizer, and improved cultivars has increased yields of major crops by 3x to 6x from 1900 to 2000.

<span class="mw-page-title-main">Organophosphate</span> Organic compounds with the structure O=P(OR)3

In organic chemistry, organophosphates (also known as phosphate esters, phosphorates(V) or OPEs) are a class of organophosphorus compounds with the general structure O=P(OR)3, a central phosphate molecule with alkyl or aromatic substituents. They can be considered as esters of phosphoric acid. Organophosphates are best known for their use as pesticides.

<span class="mw-page-title-main">MCPA</span> Organic compound used as an herbicide

MCPA is a widely used phenoxy herbicide introduced in 1945. It selectively controls broad-leaf weeds in pasture and cereal crops. The mode of action of MCPA is as an auxin, which are growth hormones that naturally exist in plants.

<span class="mw-page-title-main">Atrazine</span> Herbicide

Atrazine is a chlorinated herbicide of the triazine class. It is used to prevent pre-emergence broadleaf weeds in crops such as maize (corn), soybean and sugarcane and on turf, such as golf courses and residential lawns. Atrazine's primary manufacturer is Syngenta and it is one of the most widely used herbicides in the United States, Canadian, and Australian agriculture. Its use was banned in the European Union in 2004, when the EU found groundwater levels exceeding the limits set by regulators, and Syngenta could not show that this could be prevented nor that these levels were safe.

<span class="mw-page-title-main">Cyanuric chloride</span> Chemical compound

Cyanuric chloride is an organic compound with the formula (NCCl)3. This white solid is the chlorinated derivative of 1,3,5-triazine. It is the trimer of cyanogen chloride. Cyanuric chloride is the main precursor to the popular but controversial herbicide atrazine.

<span class="mw-page-title-main">Hexazinone</span> Chemical compound

Hexazinone is an organic compound that is used as a broad spectrum herbicide. It is a colorless solid. It exhibits some solubility in water but is highly soluble in most organic solvents except alkanes. A member of the triazine class herbicides, it is manufactured by DuPont and sold under the trade name Velpar.

1,3,5-Triazine, also called s-triazine, is an organic chemical compound with the formula (HCN)3. It is a six-membered heterocyclic aromatic ring, one of several isomeric triazines. S-triazine—the "symmetric" isomer—and its derivatives are useful in a variety of applications.

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<span class="mw-page-title-main">Pinacolone</span> Chemical compound

Pinacolone (3,3-dimethyl-2-butanone) is an important ketone in organic chemistry. It is a colorless liquid and has a slight peppermint- or camphor- odor. It is a precursor to triazolylpinacolone in the synthesis of the fungicide triadimefon and in synthesis of the herbicide metribuzin. The molecule is an unsymmetrical ketone. The α-methyl group can participate in condensation reactions. The carbonyl group can undergo the usual reactions. It is a Schedule 3 compound under the Chemical Weapons Convention 1993, due to being related to pinacolyl alcohol, which is used in the production of soman. It is also a controlled export in Australia Group member states.

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Amine alkylation (amino-dehalogenation) is a type of organic reaction between an alkyl halide and ammonia or an amine. The reaction is called nucleophilic aliphatic substitution, and the reaction product is a higher substituted amine. The method is widely used in the laboratory, but less so industrially, where alcohols are often preferred alkylating agents.

<span class="mw-page-title-main">Saflufenacil</span> Chemical compound

Saflufenacil is the ISO common name for an organic compound of the pyrimidinedione chemical class used as an herbicide. It acts by inhibiting the enzyme protoporphyrinogen oxidase to control broadleaf weeds in crops including soybeans and corn.

<span class="mw-page-title-main">2,4-Dichlorophenoxyacetic acid</span> Herbicide

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<span class="mw-page-title-main">Acifluorfen</span> Chemical compound

Acifluorfen is the ISO common name for an organic compound used as an herbicide. It acts by inhibiting the enzyme protoporphyrinogen oxidase which is necessary for chlorophyll synthesis. Soybeans naturally have a high tolerance to acifluorfen and its salts, via metabolic disposal by glutathione S-transferase. It is effective against broadleaf weeds and grasses and is used agriculturally on fields growing soybeans, peanuts, peas, and rice.

<span class="mw-page-title-main">Aram Nalbandyan</span>

Aram Bagrati "Bagratovich" Nalbandyan was a Soviet and Armenian physicist, prominent in the field of physical chemistry, founder of the Institute of Chemical Physics in Yerevan, Armenia, and academician-secretary of the Chemical Department of the Armenian Academy of Sciences (AS). He is the author of more than 400 scientific articles and five monographs.

Pesticide degradation is the process by which a pesticide is transformed into a benign substance that is environmentally compatible with the site to which it was applied. Globally, an estimated 1 to 2.5 million tons of active pesticide ingredients are used each year, mainly in agriculture. Forty percent are herbicides, followed by insecticides and fungicides. Since their initial development in the 1940s, multiple chemical pesticides with different uses and modes of action have been employed. Pesticides are applied over large areas in agriculture and urban settings. Pesticide use, therefore, represents an important source of diffuse chemical environmental inputs.

<span class="mw-page-title-main">Fluazifop</span> ACCase herbicide, fop, anti-grass

Fluazifop is the common name used by the ISO for an organic compound that is used as a selective herbicide. The active ingredient is the 2R enantiomer at its chiral centre and this material is known as fluazifop-P when used in that form. More commonly, it is sold as its butyl ester, fluazifop-P butyl with the brand name Fusilade.

<span class="mw-page-title-main">Butafenacil</span> Chemical compound

Butafenacil is the ISO common name for an organic compound of the pyrimidinedione chemical class used as an herbicide. It acts by inhibiting the enzyme protoporphyrinogen oxidase to control broadleaf and some grass weeds in crops including cereals and canola.

<span class="mw-page-title-main">Tribenuron</span> Chemical compound

Tribenuron in the form of tribenuron-methyl is a sulfonylurea herbicide. Its mode of action is the inhibition of acetolactate synthase, group 2 of the Herbicide Resistance Action Committee's classification scheme.

References

  1. 1 2 "Национальная академия наук Республики Армения". Archived from the original on 2020-09-29.
  2. 1 2 "Դովլաթյան Վռամ Վաղինակի". persons.anau.am. Archived from the original on 2021-05-07. Retrieved 2020-10-10.