Издательство СО РАН

Издательство СО РАН

Адрес Издательства СО РАН: Россия, 630090, а/я 187
Новосибирск, Морской пр., 2

soran2.gif

Baner_Nauka_Sibiri.jpg


Яндекс.Метрика

Array
(
    [SESS_AUTH] => Array
        (
            [POLICY] => Array
                (
                    [SESSION_TIMEOUT] => 24
                    [SESSION_IP_MASK] => 0.0.0.0
                    [MAX_STORE_NUM] => 10
                    [STORE_IP_MASK] => 0.0.0.0
                    [STORE_TIMEOUT] => 525600
                    [CHECKWORD_TIMEOUT] => 525600
                    [PASSWORD_LENGTH] => 6
                    [PASSWORD_UPPERCASE] => N
                    [PASSWORD_LOWERCASE] => N
                    [PASSWORD_DIGITS] => N
                    [PASSWORD_PUNCTUATION] => N
                    [LOGIN_ATTEMPTS] => 0
                    [PASSWORD_REQUIREMENTS] => Пароль должен быть не менее 6 символов длиной.
                )

        )

    [SESS_IP] => 3.139.103.103
    [SESS_TIME] => 1733301420
    [BX_SESSION_SIGN] => 9b3eeb12a31176bf2731c6c072271eb6
    [fixed_session_id] => 2a48c0275b9ab59cf4936741a093ea5d
    [UNIQUE_KEY] => 5d42d0d6cf42b13c2b7e17a42c14318b
    [BX_LOGIN_NEED_CAPTCHA_LOGIN] => Array
        (
            [LOGIN] => 
            [POLICY_ATTEMPTS] => 0
        )

)

Поиск по журналу

Журнал структурной химии

2015 год, номер 7

STRUCTURES AND ANTIMICROBIAL ACTIVITY OF FLUORO- AND HYDROXY-SUBSTITUTED THIOCARBOXYHYDRAZONES

Z.-X. Liu
School of Chemistry and Chemical Engineering, Linyi University, Linyi Shandong, P. R. China
zengxin_liu@163.com
Ключевые слова: synthesis, hiocarboxyhydrazones, antimicrobial activity, crystal structure, hydrogen bonding, synthesis, hiocarboxyhydrazones, antimicrobial activity, crystal structure, hydrogen bonding
Страницы: 1476-1480
Подраздел: КРАТКИЕ СООБЩЕНИЯ

Аннотация

A series of fluoro- and hydroxy-substituted thiocarboxyhydrazones, 2-(3-fluorobenzylidene)-N-methylhydrazinecarbothioamide (1), 2-(2,3-difluorobenzylidene)-N-methylhydrazinecarbothioamide (2), and 2-(2-hydroxybenzylidene)-N-methylhydrazinecarbothioamide (3), are synthesized and characterized by elemental analysis, IR and UV-vis spectra, and single crystal X-ray diffraction. Structures of the three compounds are similar, but with a slight modification due to fluoro substituting groups. The crystal structures of the compounds are stabilized by hydrogen bonds and π⋯π interactions. The antimicrobial activity of the compounds shows that they are effective against some bacteria.

DOI: 10.15372/JSC20150727