Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes

In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O...
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Autor*in:	Yin, Lili [verfasserIn] Zhang, Shaonan [verfasserIn] Zhou, Tao [verfasserIn] Zhen'guang, Hu [verfasserIn] Zhang, Shuhua [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2022

Schlagwörter:	Salicylaldehyde Schiff-base Anticancer activity Hirshfeld surface analyses

Übergeordnetes Werk:	Enthalten in: Journal of molecular structure - New York, NY [u.a.] : Elsevier, 1967, 1275
Übergeordnetes Werk:	volume:1275

DOI / URN:	10.1016/j.molstruc.2022.134683

Katalog-ID:	ELV009027505

Internformat


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024	7		\|a 10.1016/j.molstruc.2022.134683 \|2 doi
035			\|a (DE-627)ELV009027505
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100	1		\|a Yin, Lili \|e verfasserin \|4 aut
245	1	0	\|a Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes
264		1	\|c 2022
336			\|a nicht spezifiziert \|b zzz \|2 rdacontent
337			\|a Computermedien \|b c \|2 rdamedia
338			\|a Online-Ressource \|b cr \|2 rdacarrier
520			\|a In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells.
650		4	\|a Salicylaldehyde Schiff-base
650		4	\|a Anticancer activity
650		4	\|a Hirshfeld surface analyses
700	1		\|a Zhang, Shaonan \|e verfasserin \|4 aut
700	1		\|a Zhou, Tao \|e verfasserin \|4 aut
700	1		\|a Zhen'guang, Hu \|e verfasserin \|4 aut
700	1		\|a Zhang, Shuhua \|e verfasserin \|0 (orcid)0000-0002-1097-1674 \|4 aut
773	0	8	\|i Enthalten in \|t Journal of molecular structure \|d New York, NY [u.a.] : Elsevier, 1967 \|g 1275 \|h Online-Ressource \|w (DE-627)302469745 \|w (DE-600)1491504-2 \|w (DE-576)255266626 \|x 0022-2860 \|7 nnns
773	1	8	\|g volume:1275
912			\|a GBV_USEFLAG_U
912			\|a SYSFLAG_U
912			\|a GBV_ELV
912			\|a SSG-OLC-PHA
912			\|a GBV_ILN_20
912			\|a GBV_ILN_22
912			\|a GBV_ILN_23
912			\|a GBV_ILN_24
912			\|a GBV_ILN_31
912			\|a GBV_ILN_32
912			\|a GBV_ILN_40
912			\|a GBV_ILN_60
912			\|a GBV_ILN_62
912			\|a GBV_ILN_63
912			\|a GBV_ILN_65
912			\|a GBV_ILN_69
912			\|a GBV_ILN_70
912			\|a GBV_ILN_73
912			\|a GBV_ILN_74
912			\|a GBV_ILN_90
912			\|a GBV_ILN_95
912			\|a GBV_ILN_100
912			\|a GBV_ILN_101
912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_150
912			\|a GBV_ILN_151
912			\|a GBV_ILN_224
912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_702
912			\|a GBV_ILN_2003
912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_2015
912			\|a GBV_ILN_2020
912			\|a GBV_ILN_2021
912			\|a GBV_ILN_2025
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2038
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
912			\|a GBV_ILN_2049
912			\|a GBV_ILN_2050
912			\|a GBV_ILN_2056
912			\|a GBV_ILN_2059
912			\|a GBV_ILN_2061
912			\|a GBV_ILN_2064
912			\|a GBV_ILN_2065
912			\|a GBV_ILN_2068
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_2112
912			\|a GBV_ILN_2113
912			\|a GBV_ILN_2118
912			\|a GBV_ILN_2122
912			\|a GBV_ILN_2129
912			\|a GBV_ILN_2143
912			\|a GBV_ILN_2147
912			\|a GBV_ILN_2148
912			\|a GBV_ILN_2152
912			\|a GBV_ILN_2153
912			\|a GBV_ILN_2190
912			\|a GBV_ILN_2336
912			\|a GBV_ILN_2507
912			\|a GBV_ILN_2522
912			\|a GBV_ILN_4035
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4126
912			\|a GBV_ILN_4242
912			\|a GBV_ILN_4251
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4323
912			\|a GBV_ILN_4324
912			\|a GBV_ILN_4326
912			\|a GBV_ILN_4333
912			\|a GBV_ILN_4334
912			\|a GBV_ILN_4335
912			\|a GBV_ILN_4338
912			\|a GBV_ILN_4393
936	b	k	\|a 35.00 \|j Chemie: Allgemeines
951			\|a AR
952			\|d 1275

Indexfelder

author_variant	l y ly s z sz t z tz h z hz s z sz
matchkey_str	article:00222860:2022----::yteicaatrztoadniacrciiyfooulas
hierarchy_sort_str	2022
bklnumber	35.00
publishDate	2022
allfields	10.1016/j.molstruc.2022.134683 doi (DE-627)ELV009027505 (ELSEVIER)S0022-2860(22)02328-6 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Yin, Lili verfasserin aut Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells. Salicylaldehyde Schiff-base Anticancer activity Hirshfeld surface analyses Zhang, Shaonan verfasserin aut Zhou, Tao verfasserin aut Zhen'guang, Hu verfasserin aut Zhang, Shuhua verfasserin (orcid)0000-0002-1097-1674 aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1275 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1275 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1275
spelling	10.1016/j.molstruc.2022.134683 doi (DE-627)ELV009027505 (ELSEVIER)S0022-2860(22)02328-6 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Yin, Lili verfasserin aut Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells. Salicylaldehyde Schiff-base Anticancer activity Hirshfeld surface analyses Zhang, Shaonan verfasserin aut Zhou, Tao verfasserin aut Zhen'guang, Hu verfasserin aut Zhang, Shuhua verfasserin (orcid)0000-0002-1097-1674 aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1275 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1275 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1275
allfields_unstemmed	10.1016/j.molstruc.2022.134683 doi (DE-627)ELV009027505 (ELSEVIER)S0022-2860(22)02328-6 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Yin, Lili verfasserin aut Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells. Salicylaldehyde Schiff-base Anticancer activity Hirshfeld surface analyses Zhang, Shaonan verfasserin aut Zhou, Tao verfasserin aut Zhen'guang, Hu verfasserin aut Zhang, Shuhua verfasserin (orcid)0000-0002-1097-1674 aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1275 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1275 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1275
allfieldsGer	10.1016/j.molstruc.2022.134683 doi (DE-627)ELV009027505 (ELSEVIER)S0022-2860(22)02328-6 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Yin, Lili verfasserin aut Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells. Salicylaldehyde Schiff-base Anticancer activity Hirshfeld surface analyses Zhang, Shaonan verfasserin aut Zhou, Tao verfasserin aut Zhen'guang, Hu verfasserin aut Zhang, Shuhua verfasserin (orcid)0000-0002-1097-1674 aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1275 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1275 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1275
allfieldsSound	10.1016/j.molstruc.2022.134683 doi (DE-627)ELV009027505 (ELSEVIER)S0022-2860(22)02328-6 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Yin, Lili verfasserin aut Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells. Salicylaldehyde Schiff-base Anticancer activity Hirshfeld surface analyses Zhang, Shaonan verfasserin aut Zhou, Tao verfasserin aut Zhen'guang, Hu verfasserin aut Zhang, Shuhua verfasserin (orcid)0000-0002-1097-1674 aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1275 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1275 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1275
language	English
source	Enthalten in Journal of molecular structure 1275 volume:1275
sourceStr	Enthalten in Journal of molecular structure 1275 volume:1275
format_phy_str_mv	Article
bklname	Chemie: Allgemeines
institution	findex.gbv.de
topic_facet	Salicylaldehyde Schiff-base Anticancer activity Hirshfeld surface analyses
dewey-raw	540
isfreeaccess_bool	false
container_title	Journal of molecular structure
authorswithroles_txt_mv	Yin, Lili @@aut@@ Zhang, Shaonan @@aut@@ Zhou, Tao @@aut@@ Zhen'guang, Hu @@aut@@ Zhang, Shuhua @@aut@@
publishDateDaySort_date	2022-01-01T00:00:00Z
hierarchy_top_id	302469745
dewey-sort	3540
id	ELV009027505
language_de	englisch
fullrecord	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV009027505</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230524155421.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230510s2022 xx \|\|\|\|\|o 00\| \|\|eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.molstruc.2022.134683</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV009027505</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0022-2860(22)02328-6</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">35.00</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Yin, Lili</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2022</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. 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author	Yin, Lili
spellingShingle	Yin, Lili ddc 540 bkl 35.00 misc Salicylaldehyde Schiff-base misc Anticancer activity misc Hirshfeld surface analyses Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes
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topic_title	540 DE-600 35.00 bkl Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes Salicylaldehyde Schiff-base Anticancer activity Hirshfeld surface analyses
topic	ddc 540 bkl 35.00 misc Salicylaldehyde Schiff-base misc Anticancer activity misc Hirshfeld surface analyses
topic_unstemmed	ddc 540 bkl 35.00 misc Salicylaldehyde Schiff-base misc Anticancer activity misc Hirshfeld surface analyses
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title	Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes
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title_full	Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes
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author_browse	Yin, Lili Zhang, Shaonan Zhou, Tao Zhen'guang, Hu Zhang, Shuhua
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author-letter	Yin, Lili
doi_str_mv	10.1016/j.molstruc.2022.134683
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title_sort	synthesis, characterization, and anticancer activity of mononuclear schiff-base metal complexes
title_auth	Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes
abstract	In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells.
abstractGer	In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells.
abstract_unstemmed	In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells.
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title_short	Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes
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author2	Zhang, Shaonan Zhou, Tao Zhen'guang, Hu Zhang, Shuhua
author2Str	Zhang, Shaonan Zhou, Tao Zhen'guang, Hu Zhang, Shuhua
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doi_str	10.1016/j.molstruc.2022.134683
up_date	2024-07-06T21:44:11.678Z
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fullrecord_marcxml	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV009027505</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230524155421.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230510s2022 xx \|\|\|\|\|o 00\| \|\|eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.molstruc.2022.134683</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV009027505</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0022-2860(22)02328-6</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">35.00</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Yin, Lili</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2022</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">In this study, 9 transition metal complexes, namely, [M(HL n)2]·0.5(H2O) (1, M = Ni, n = i; 2, M = Zn, n = i; 3, M = Ni, n = ii; 7, M = Zn, n = iv); [M(HL n)2]·0.25(H2O) (4, M = Zn, n = ii; 8, M = Ni, n = v); [Zn(HLiii )2]·DMF·H2O (5); [Ni(HL iv)2]·0.5(C2H5OH) (6), Zn(HL v)2 (9) (H2Li  = (E)-4‑chloro-2-((2- (6-chloropyridin-2-yl)hydrazineylidene)methyl)phenol; H2Lii  = (E)-4‑bromo-2-((2-(6-chloropyridin- 2-yl)hydrazineylidene)methyl)phenol; H2Liii  = (E)-2,4-dibromo-6-((2-(6-chloropyridin-2-yl) hydrazineylidene)methyl)phenol; H2Liv  = (E)-2-((2-(6-bromopyridin-2-yl)hydrazineylidene)methyl)- 4-chlorophenol; H2Lv  = (E)-4‑bromo-2-((2-(6-bromopyridin-2-yl) hydrazineylidene)methyl)phenol; DMF = N,N-dimethylformamide) were synthesized and characterized by Elemental analysis (EA), Infrared spectroscopy (IR), Single-crystal X-ray diffraction (SC-XRD) and Hirshfeld surface analyses. Moreover, we also investigated the anticancer effects of these 9 structures by standard MTT assay. Anticancer activity studies have shown that these metal complexes play a role in inhibiting the growth of cancer cells.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Salicylaldehyde Schiff-base</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Anticancer activity</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Hirshfeld surface analyses</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhang, Shaonan</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhou, Tao</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhen'guang, Hu</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" 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Synthesis, characterization, and anticancer activity of mononuclear Schiff-base metal complexes

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