Copper–Bispidine Complexes: Synthesis and Complex Stability Study

A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper­(II) complexes suitable as imaging agents for positron emission tomography. For characterization purposes, copper complexes of bispidines were synthesized in the pure form and in quantitative yields...

Full description

Saved in:
Bibliographic Details
Published inACS omega Vol. 1; no. 5; pp. 854 - 867
Main Authors Medved’ko, Aleksei V, Egorova, Bayirta V, Komarova, Alina A, Rakhimov, Rustem D, Krut’ko, Dmitri P, Kalmykov, Stepan N, Vatsadze, Sergey Z
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 30.11.2016
Online AccessGet full text

Cover

Loading…
Abstract A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper­(II) complexes suitable as imaging agents for positron emission tomography. For characterization purposes, copper complexes of bispidines were synthesized in the pure form and in quantitative yields by neutralization of ligands with malachite. The formation of complexes and their stoichiometries were studied by potentiometric titration, cyclic voltammetry, and spectroscopic methods. The stability constants were found to be fairly suitable for copper cation fixation inside dianionic chelate molecules.
AbstractList A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper(II) complexes suitable as imaging agents for positron emission tomography. For characterization purposes, copper complexes of bispidines were synthesized in the pure form and in quantitative yields by neutralization of ligands with malachite. The formation of complexes and their stoichiometries were studied by potentiometric titration, cyclic voltammetry, and spectroscopic methods. The stability constants were found to be fairly suitable for copper cation fixation inside dianionic chelate molecules.A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper(II) complexes suitable as imaging agents for positron emission tomography. For characterization purposes, copper complexes of bispidines were synthesized in the pure form and in quantitative yields by neutralization of ligands with malachite. The formation of complexes and their stoichiometries were studied by potentiometric titration, cyclic voltammetry, and spectroscopic methods. The stability constants were found to be fairly suitable for copper cation fixation inside dianionic chelate molecules.
A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper(II) complexes suitable as imaging agents for positron emission tomography. For characterization purposes, copper complexes of bispidines were synthesized in the pure form and in quantitative yields by neutralization of ligands with malachite. The formation of complexes and their stoichiometries were studied by potentiometric titration, cyclic voltammetry, and spectroscopic methods. The stability constants were found to be fairly suitable for copper cation fixation inside dianionic chelate molecules.
A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper­(II) complexes suitable as imaging agents for positron emission tomography. For characterization purposes, copper complexes of bispidines were synthesized in the pure form and in quantitative yields by neutralization of ligands with malachite. The formation of complexes and their stoichiometries were studied by potentiometric titration, cyclic voltammetry, and spectroscopic methods. The stability constants were found to be fairly suitable for copper cation fixation inside dianionic chelate molecules.
A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper(II) complexes suitable as imaging agents for positron emission tomography. For characterization purposes, copper complexes of bispidines were synthesized in the pure form and in quantitative yields by neutralization of ligands with malachite. The formation of complexes and their stoichiometries were studied by potentiometric titration, cyclic voltammetry, and spectroscopic methods. The stability constants were found to be fairly suitable for copper cation fixation inside dianionic chelate molecules.
Author Rakhimov, Rustem D
Egorova, Bayirta V
Komarova, Alina A
Medved’ko, Aleksei V
Kalmykov, Stepan N
Krut’ko, Dmitri P
Vatsadze, Sergey Z
AuthorAffiliation Faculty of Chemistry
Lomonosov Moscow State University
Faculty of Materials Science
AuthorAffiliation_xml – name: Faculty of Materials Science
– name: Faculty of Chemistry
– name: Lomonosov Moscow State University
Author_xml – sequence: 1
  givenname: Aleksei V
  surname: Medved’ko
  fullname: Medved’ko, Aleksei V
– sequence: 2
  givenname: Bayirta V
  surname: Egorova
  fullname: Egorova, Bayirta V
– sequence: 3
  givenname: Alina A
  surname: Komarova
  fullname: Komarova, Alina A
– sequence: 4
  givenname: Rustem D
  surname: Rakhimov
  fullname: Rakhimov, Rustem D
– sequence: 5
  givenname: Dmitri P
  surname: Krut’ko
  fullname: Krut’ko, Dmitri P
– sequence: 6
  givenname: Stepan N
  surname: Kalmykov
  fullname: Kalmykov, Stepan N
– sequence: 7
  givenname: Sergey Z
  surname: Vatsadze
  fullname: Vatsadze, Sergey Z
  email: szv@org.chem.msu.ru
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31457168$$D View this record in MEDLINE/PubMed
BookMark eNp9kUFvFCEUx4lpY2vt3ZPZowe3BYYBxoOJTtQ2aeKheibAPLZsZoYRGOPe_A5-Qz-J1N1tWpN64vHe__97kP8zdDCGERB6QfAZwZSca5vCACt9xg3GtBJP0DFlAi9JxaqDe_UROk1pjTEmXFJJ-VN0VBFWi3I9Rm0bpgni75-_3vs0-c6PsGjDMPXwA9KbxfVmzDeQfFrosdsPFtdZG9_7vCnV3G2eo0On-wSnu_MEff344Ut7sbz6_OmyfXe11Kxp8hIENBWm3AkMnal1ZVklraCMSgfSdg5qyiU0DQgJknEKoiHQWKcNo4bI6gRdbrld0Gs1RT_ouFFBe_W3EeJK6Zi97UEZQSwzphZSCGZNLZ0A6qjDgrGqca6w3m5Z02wG6CyMOer-AfThZPQ3ahW-K85ZgfACeLUDxPBthpTV4JOFvtcjhDkpSiUpnyCcFunL-7vuluxTKAK8FdgYUorg7iQEq9us1T5rtcu6WPg_Fuuzzj7cvtb3_zO-3hrLRK3DHMcS2ePyP6DpwOY
CitedBy_id crossref_primary_10_1070_RCR5011
crossref_primary_10_1007_s10593_020_02643_2
crossref_primary_10_1021_acsmedchemlett_1c00299
crossref_primary_10_1002_cplu_201800110
crossref_primary_10_1016_j_mencom_2021_04_023
crossref_primary_10_1039_D0CE01730B
crossref_primary_10_1107_S2056989017009458
crossref_primary_10_1021_acs_oprd_4c00086
crossref_primary_10_3390_molecules30051138
crossref_primary_10_1039_C8DT01108G
crossref_primary_10_3390_molecules27020430
crossref_primary_10_1080_17518253_2024_2391919
crossref_primary_10_1007_s11172_021_3180_9
crossref_primary_10_3390_nano9010089
crossref_primary_10_31857_S0514749223030096
crossref_primary_10_1134_S1070428023030090
crossref_primary_10_1002_jlcr_3728
crossref_primary_10_1007_s11172_024_4143_8
crossref_primary_10_1134_S107042801802001X
crossref_primary_10_1039_D5DT00050E
crossref_primary_10_1007_s11172_023_3729_x
crossref_primary_10_1021_acs_joc_3c00514
crossref_primary_10_1016_j_ica_2017_08_022
crossref_primary_10_1007_s11172_024_4241_7
crossref_primary_10_1016_j_tetlet_2017_10_069
crossref_primary_10_1016_j_jorganchem_2021_121945
Cites_doi 10.1021/ic4004214
10.1016/j.jinorgbio.2015.05.009
10.1007/BF01164742
10.1002/9780470144428.ch9
10.1002/jhet.5570150603
10.1088/0031-9155/59/23/7419
10.1021/acs.inorgchem.5b02855
10.1021/ic0513383
10.1158/1078-0432.CCR-10-0382
10.2174/1568026615666150915111434
10.1007/BF00475254
10.1135/cccc19733491
10.1016/j.addr.2012.10.012
10.1021/ed074p1463
10.1039/C3CS60304K
10.1517/17460441.2.5.659
10.1007/s11172-008-0303-5
10.2310/7290.2010.00008
10.1002/anie.200800515
10.1073/pnas.0705347104
10.1038/nprot.2006.431
10.1021/ic2019296
10.1007/s11172-014-0526-6
10.1007/s11172-006-0044-2
10.1071/CH09321
10.1021/ic4008685
10.1021/acs.inorgchem.5b00207
10.1021/jm030383m
10.1002/cber.19590921042
10.1016/S0039-9140(99)00245-3
10.1039/C4DT03262D
10.1021/ic500476u
10.1021/ic011114u
10.1107/S0108270198099661
10.1021/ic061501+
10.1021/jo0604991
10.1039/dt9950003705
10.1016/0039-9140(96)01958-3
10.1016/j.tet.2015.02.076
10.1023/A:1002820816850
10.1149/1.1838036
10.1021/jo00949a006
10.1007/BF00474490
10.1021/cr3003104
10.1021/jo01265a073
10.1021/om9609527
10.1039/C39740000725
10.1016/j.ccr.2006.10.007
10.1002/chem.201404086
10.1039/c1dt10379b
10.1016/j.ica.2012.01.061
10.1016/S0022-328X(99)00447-7
10.1007/BF00842964
10.1007/978-3-540-49527-7_6
10.2967/jnumed.108.051326
10.1002/chem.200701910
10.1016/j.mencom.2016.03.001
10.1016/0040-4020(73)80114-0
10.1007/s00775-006-0161-2
10.1007/BF02741595
10.1039/c39740000750
10.1021/bc990167l
10.1007/s11172-014-0800-7
10.1007/s00259-003-1413-9
10.1016/S0969-8051(98)00049-3
10.1016/j.apradiso.2007.05.012
10.1039/c39940001363
10.1016/0040-4020(94)01069-C
10.1016/0040-4020(76)80122-6
10.1023/B:RUEL.0000003455.12268.e2
10.2967/jnumed.107.039487
10.1016/0003-2670(96)00200-0
10.1039/a603635j
10.1021/ic102430a
10.1007/BF00702383
ContentType Journal Article
Copyright Copyright © 2016 American Chemical Society
Copyright © 2016 American Chemical Society 2016 American Chemical Society
Copyright_xml – notice: Copyright © 2016 American Chemical Society
– notice: Copyright © 2016 American Chemical Society 2016 American Chemical Society
DBID N~.
AAYXX
CITATION
NPM
7X8
5PM
DOA
DOI 10.1021/acsomega.6b00237
DatabaseName American Chemical Society (ACS) Open Access
CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic


PubMed
Database_xml – sequence: 1
  dbid: N~.
  name: American Chemical Society (ACS) Open Access
  url: https://pubs.acs.org
  sourceTypes: Publisher
– sequence: 2
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 3
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 2470-1343
EndPage 867
ExternalDocumentID oai_doaj_org_article_b71c4bb578774cb58f7e2f2f074439ff
PMC6640746
31457168
10_1021_acsomega_6b00237
b125788274
Genre Journal Article
GroupedDBID 53G
ABUCX
ACS
ADACO
ADBBV
AFEFF
ALMA_UNASSIGNED_HOLDINGS
BCNDV
EBS
EJD
GROUPED_DOAJ
HYE
N~.
OK1
ROL
RPM
VF5
AAFWJ
AAHBH
AAYXX
ABBLG
ADUCK
AFPKN
AOIJS
CITATION
M~E
NPM
7X8
5PM
ID FETCH-LOGICAL-a499t-e7e93026f70edb5a3c438c72428fe8cdfe5268e99e78e8462e791e9cfab42b183
IEDL.DBID DOA
ISSN 2470-1343
IngestDate Wed Aug 27 01:19:48 EDT 2025
Thu Aug 21 14:10:41 EDT 2025
Thu Jul 10 20:40:56 EDT 2025
Mon Jul 21 06:02:44 EDT 2025
Thu Apr 24 23:01:55 EDT 2025
Tue Jul 01 01:21:02 EDT 2025
Thu Aug 27 13:42:37 EDT 2020
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 5
Language English
License http://pubs.acs.org/page/policy/authorchoice_termsofuse.html
This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-a499t-e7e93026f70edb5a3c438c72428fe8cdfe5268e99e78e8462e791e9cfab42b183
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://doaj.org/article/b71c4bb578774cb58f7e2f2f074439ff
PMID 31457168
PQID 2281846162
PQPubID 23479
PageCount 14
ParticipantIDs doaj_primary_oai_doaj_org_article_b71c4bb578774cb58f7e2f2f074439ff
pubmedcentral_primary_oai_pubmedcentral_nih_gov_6640746
proquest_miscellaneous_2281846162
pubmed_primary_31457168
crossref_primary_10_1021_acsomega_6b00237
crossref_citationtrail_10_1021_acsomega_6b00237
acs_journals_10_1021_acsomega_6b00237
ProviderPackageCode ACS
ABUCX
AFEFF
VF5
N~.
CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2016-11-30
PublicationDateYYYYMMDD 2016-11-30
PublicationDate_xml – month: 11
  year: 2016
  text: 2016-11-30
  day: 30
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle ACS omega
PublicationTitleAlternate ACS Omega
PublicationYear 2016
Publisher American Chemical Society
Publisher_xml – name: American Chemical Society
References ref9/cit9
ref45/cit45
ref27/cit27
ref63/cit63
ref56/cit56
ref16/cit16
ref52/cit52
ref23/cit23
ref8/cit8
ref31/cit31
ref59/cit59
ref2/cit2
ref77/cit77
ref34/cit34
ref71/cit71
ref37/cit37
Welch M. J. (ref3/cit3) 2007
ref20/cit20
ref48/cit48
ref60/cit60
ref74/cit74
ref17/cit17
ref10/cit10
ref35/cit35
ref53/cit53
ref19/cit19
ref21/cit21
ref42/cit42
ref46/cit46
ref49/cit49
ref13/cit13
ref61/cit61
ref75/cit75
ref67/cit67
ref24/cit24
ref38/cit38
ref50/cit50
ref64/cit64
ref78/cit78
ref54/cit54
ref6/cit6
ref36/cit36
Lewis J. S. (ref7/cit7) 2002; 43
ref18/cit18
ref65/cit65
ref11/cit11
ref25/cit25
ref29/cit29
ref72/cit72
ref76/cit76
ref32/cit32
ref39/cit39
ref14/cit14
ref57/cit57
ref5/cit5
ref51/cit51
ref43/cit43
ref28/cit28
ref40/cit40
ref68/cit68
ref26/cit26
ref55/cit55
ref73/cit73
ref69/cit69
ref12/cit12
ref15/cit15
ref62/cit62
ref66/cit66
ref41/cit41
ref58/cit58
ref22/cit22
ref33/cit33
ref4/cit4
ref30/cit30
ref47/cit47
ref1/cit1
ref44/cit44
ref70/cit70
References_xml – ident: ref35/cit35
  doi: 10.1021/ic4004214
– ident: ref21/cit21
  doi: 10.1016/j.jinorgbio.2015.05.009
– ident: ref47/cit47
  doi: 10.1007/BF01164742
– ident: ref34/cit34
  doi: 10.1002/9780470144428.ch9
– ident: ref43/cit43
  doi: 10.1002/jhet.5570150603
– ident: ref1/cit1
  doi: 10.1088/0031-9155/59/23/7419
– ident: ref51/cit51
  doi: 10.1021/acs.inorgchem.5b02855
– ident: ref31/cit31
  doi: 10.1021/ic0513383
– ident: ref39/cit39
  doi: 10.1158/1078-0432.CCR-10-0382
– ident: ref37/cit37
  doi: 10.2174/1568026615666150915111434
– ident: ref44/cit44
  doi: 10.1007/BF00475254
– ident: ref64/cit64
  doi: 10.1135/cccc19733491
– ident: ref6/cit6
  doi: 10.1016/j.addr.2012.10.012
– ident: ref76/cit76
  doi: 10.1021/ed074p1463
– ident: ref4/cit4
  doi: 10.1039/C3CS60304K
– ident: ref13/cit13
  doi: 10.1517/17460441.2.5.659
– ident: ref50/cit50
  doi: 10.1007/s11172-008-0303-5
– ident: ref69/cit69
– ident: ref2/cit2
  doi: 10.2310/7290.2010.00008
– ident: ref27/cit27
  doi: 10.1002/anie.200800515
– ident: ref73/cit73
  doi: 10.1073/pnas.0705347104
– ident: ref71/cit71
  doi: 10.1038/nprot.2006.431
– ident: ref28/cit28
  doi: 10.1021/ic2019296
– ident: ref18/cit18
  doi: 10.1007/s11172-014-0526-6
– ident: ref19/cit19
  doi: 10.1007/s11172-006-0044-2
– ident: ref30/cit30
  doi: 10.1071/CH09321
– ident: ref12/cit12
– ident: ref36/cit36
  doi: 10.1021/ic4008685
– ident: ref41/cit41
  doi: 10.1021/acs.inorgchem.5b00207
– ident: ref75/cit75
  doi: 10.1021/jm030383m
– ident: ref62/cit62
  doi: 10.1002/cber.19590921042
– ident: ref77/cit77
  doi: 10.1016/S0039-9140(99)00245-3
– ident: ref24/cit24
  doi: 10.1039/C4DT03262D
– ident: ref26/cit26
  doi: 10.1021/ic500476u
– ident: ref32/cit32
  doi: 10.1021/ic011114u
– ident: ref14/cit14
  doi: 10.1107/S0108270198099661
– ident: ref23/cit23
  doi: 10.1021/ic061501+
– ident: ref58/cit58
  doi: 10.1021/jo0604991
– ident: ref61/cit61
  doi: 10.1039/dt9950003705
– ident: ref78/cit78
  doi: 10.1016/0039-9140(96)01958-3
– ident: ref45/cit45
  doi: 10.1016/j.tet.2015.02.076
– ident: ref17/cit17
  doi: 10.1023/A:1002820816850
– ident: ref70/cit70
  doi: 10.1149/1.1838036
– ident: ref63/cit63
  doi: 10.1021/jo00949a006
– ident: ref49/cit49
  doi: 10.1007/BF00474490
– ident: ref5/cit5
  doi: 10.1021/cr3003104
– ident: ref56/cit56
  doi: 10.1021/jo01265a073
– ident: ref57/cit57
  doi: 10.1021/om9609527
– ident: ref66/cit66
  doi: 10.1039/C39740000725
– ident: ref38/cit38
  doi: 10.1016/j.ccr.2006.10.007
– ident: ref33/cit33
  doi: 10.1002/chem.201404086
– ident: ref53/cit53
  doi: 10.1039/c1dt10379b
– ident: ref54/cit54
  doi: 10.1016/j.ica.2012.01.061
– ident: ref16/cit16
  doi: 10.1016/S0022-328X(99)00447-7
– ident: ref48/cit48
  doi: 10.1007/BF00842964
– start-page: 159
  volume-title: PET Chemistry: The Driving Force in Molecular Imaging
  year: 2007
  ident: ref3/cit3
  doi: 10.1007/978-3-540-49527-7_6
– ident: ref8/cit8
  doi: 10.2967/jnumed.108.051326
– ident: ref22/cit22
  doi: 10.1002/chem.200701910
– ident: ref11/cit11
  doi: 10.1016/j.mencom.2016.03.001
– ident: ref67/cit67
  doi: 10.1016/0040-4020(73)80114-0
– ident: ref29/cit29
  doi: 10.1007/s00775-006-0161-2
– ident: ref46/cit46
  doi: 10.1007/BF02741595
– ident: ref65/cit65
  doi: 10.1039/c39740000750
– ident: ref74/cit74
  doi: 10.1021/bc990167l
– ident: ref42/cit42
  doi: 10.1007/s11172-014-0800-7
– ident: ref40/cit40
  doi: 10.1007/s00259-003-1413-9
– ident: ref9/cit9
  doi: 10.1016/S0969-8051(98)00049-3
– ident: ref10/cit10
  doi: 10.1016/j.apradiso.2007.05.012
– ident: ref60/cit60
  doi: 10.1039/c39940001363
– ident: ref52/cit52
  doi: 10.1016/0040-4020(94)01069-C
– ident: ref68/cit68
  doi: 10.1016/0040-4020(76)80122-6
– ident: ref15/cit15
  doi: 10.1023/B:RUEL.0000003455.12268.e2
– ident: ref72/cit72
  doi: 10.2967/jnumed.107.039487
– volume: 43
  start-page: 1557
  year: 2002
  ident: ref7/cit7
  publication-title: J. Nucl. Med.
– ident: ref59/cit59
  doi: 10.1016/0003-2670(96)00200-0
– ident: ref20/cit20
  doi: 10.1039/a603635j
– ident: ref25/cit25
  doi: 10.1021/ic102430a
– ident: ref55/cit55
  doi: 10.1007/BF00702383
SSID ssj0001682826
Score 2.13829
Snippet A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper­(II) complexes suitable as imaging agents for positron...
A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper(II) complexes suitable as imaging agents for positron...
A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper(II) complexes suitable as imaging agents for positron...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
acs
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 854
SummonAdditionalLinks – databaseName: American Chemical Society (ACS) Open Access
  dbid: N~.
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1LT9wwELYoHOgF8SpseSiVyoFDADuOH9xgBUJI5VKQuFm2My4rQXZFFql7qfof-If8EsbZZGERQlzjOInnkfkm43xDyE-pnBYKaFpwq1MOgaU2R4XI4BzagCiAx7-Rf12Isyt-fp1fv9DkvK3gM7pvfdW_gz92T9QBRn4hc0woFZ3w4t_ey_cUgblD3V2NcXmQ0oxnTVXyvYvEWOSrqVhUU_a_hzPfbpd8FX9OF8lCAxyTo7Gml8gMlMtkvtv2a1sh3W5_MID7p_-Px71q0MOYBEn09lv4C9Vh8ntUItarelViy6IdSBBr1rtjR0ncUDhaJVenJ5fds7RpkZBaTFWGKUjQGaZRQR5A4XKbeZ4pLzHuqgDKFwEinQtoDVIBQg0GUlPQPljHmUN3_kZmy34J6yRhWgTunccBxXUhXOGt1ZR7zKFwBuuQHRSZaUy8MnX1mlHTitY0ou2Q_Vaoxjc847Hdxe0HM3YnMwZjjo0Pzj2OepqcF9mx6wNoMqZxNuMk9dy5-DKSuKRcBQkssIBwCfFXCB3yo9WyQSXFEoktof9QGRbJsbigApe7Ntb65FYZ5Tlml6pD5JQ9TD3L9EjZu6kZu0Usl3Lx_ZMi3CBfEZeJMcPkJpkd3j_AFmKfoduujf4ZbNoCzg
  priority: 102
  providerName: American Chemical Society
Title Copper–Bispidine Complexes: Synthesis and Complex Stability Study
URI http://dx.doi.org/10.1021/acsomega.6b00237
https://www.ncbi.nlm.nih.gov/pubmed/31457168
https://www.proquest.com/docview/2281846162
https://pubmed.ncbi.nlm.nih.gov/PMC6640746
https://doaj.org/article/b71c4bb578774cb58f7e2f2f074439ff
Volume 1
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NTtwwELYqLu0FQVtgW4pSqT1wCEu8jn-4lQiEKsEFkLhZtjOGlSC7IovEXhDvwBvyJIydZLWLKnrh4kNsK87MON9MZvKZkF9CWsUlZGnJjEoZeJqaHBUivLVoA7wEFv5GPj7hR-fs70V-MXfUV6gJa-iBG8H1rcgcszYYlmDO5tILoJ56hD7EUu_D2xcxby6Yil9XOEYStMtLIo71jatHN3BpdnjEqYhGrl5Ao0ja_y9P83XB5BwCHa6Q5dZ1TP40S14lH6D6TD4W3YltX0hRjMZjuH1-fNof1uMhohIkYb9fwz3Ue8nptEJvrx7WianKriNBbzPWx06TUFI4_UrODw_OiqO0PSQhNRisTFIQoAYYSHmxC6XNzcCxgXQCkVd6kK70EAhdQCkQEtDZoCBUBsp5Yxm1uKHXyFI1qmCDJFRxjyJ22CGZKrktnTEqYw6jKJxBe-Q3iky3Rl7rmL-mme5Eq1vR9ki_E6p2LdN4OPDi-o0Z27MZ44Zl442x-0FPs3GBHzteQKvRrdXo_1lNj_zstKxRSSFJYioY3dWaBnosxjOOj7veaH12q0HGcowvZY-IBXtYWMtiTzW8ipzdPCRMGf_2Hov_Tj6h28YbAspNsjS5vYMf6BpN7BaGBsXpVtwL2B4_HGB78rDzAib3E0w
linkProvider Directory of Open Access Journals
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwEB6VcigXxLvLM0j0wCFt4zh2jMSBLlRb-rjQSr0Z2xnDSiW7qreCvSD-A7-Av8YvYZxNtiyqKi69xnFizyPzTWY8A_BCllaJErO04kalHD1LTUEMkd5akgFRIY-nkfcPxOCIvz8ujpfgV3cWhhYR6EmhCeKfVxfINuja6At-MuuisTOyzaPcxelX8tLC6523xNI1xrbfHfYHadtIIDUE6CcpSlQ5ORtebmJlC5M7npdOknUqPZau8hiLnqBSKEskg8xQqgyV88ZyZkno6bnX4DphnyLq_sH39fPfOIJclqapG-NyM81ynrfB0IsWHU2gCwsmsOkUcBG8_TdL8y-zt30LbrZ4NXkzE7DbsIT1HVjpd23i7kK_PxqP8fT3j59bwzAekinEJH5kTvAbhlfJh2lNEDMMQ2LqqhtICOI2SbnTJOYxTu_B0ZUQ9D4s16MaVyFhSnjurKOBkqtK2MoZozLuyHWjGawHa0Qy3WpW0E3QnGW6I61uSduDjY6o2rXlzWOXjZNLZryczxjPSntccu9W5NP8vliUu7lAYqpbHddWZo5bG7-BkrZUlF4i88wTSiPY530Pnndc1sSkGJkxNY7OgmaxJhcXmaDtPphxff6qPOMFObVlD-SCPCysZXGkHn5uCoWLGKXl4uF_kvAZrAwO9_f03s7B7iO4QdBQzIpcPoblyekZPiH4NbFPGwVI4ONVa9wf_glDEw
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3NbtQwELZKkYAL4p_lN0j0wCHtxnHsGIkD3bJqKayQoFJvru2M6UptNqq3gr0g3oFn4MV4EsZZZ2FRVXHpNY4Te34y32TGM4Q8F6WRvIQsrZiWKQNHU10gQ4QzBmWAV8DCaeT3I769x97uF_sr5Gd3FgYX4fFJvg3iB61uKhcrDGQbeH1yDJ_1Om9tjYi5lLsw-4Kemn-1s4VsXaN0-ObTYDuNzQRSjaB-moIAmaPD4UQfKlPo3LK8tAItVOmgtJWDUPgEpARRAhplCkJmIK3ThlGDgo_PvUQuI_rpB_0ffVv_8yuHo9vSNnajTPTTLGd5DIietehgBq1fMoNtt4CzIO6_mZp_mb7hDXI9Ytbk9VzIbpIVqG-Rq4OuVdxtMhhMmgZOfn3_sTn2zRjNISThQ3MEX8G_TD7OaoSZfuwTXVfdQIIwt03MnSUhl3F2h-xdCEHvktV6UsN9klDJHbPG4kDJZMVNZbWWGbPovuEM2iNrSDIVtcurNnBOM9WRVkXS9shGR1RlY4nz0Gnj6JwZLxYzmnl5j3Pu3Qx8WtwXCnO3F1BUVdRzZURmmTHhOyhwS0XpBFBHHSI1hH7O9cizjssKmRSiM7qGyalXNNTlYjzjuN17c64vXpVnrEDHtuwRsSQPS2tZHqnHh22xcB4itYw_-E8SPiVXPmwN1bud0e5Dcg3RIZ_XuXxEVqcnp_AYEdjUPGnlPyEHF61wvwGmnUQg
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Copper%E2%80%93Bispidine+Complexes%3A+Synthesis+and+Complex+Stability+Study&rft.jtitle=ACS+omega&rft.au=Aleksei+V.+Medved%E2%80%99ko&rft.au=Bayirta+V.+Egorova&rft.au=Alina+A.+Komarova&rft.au=Rustem+D.+Rakhimov&rft.date=2016-11-30&rft.pub=American+Chemical+Society&rft.eissn=2470-1343&rft.volume=1&rft.issue=5&rft.spage=854&rft.epage=867&rft_id=info:doi/10.1021%2Facsomega.6b00237&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_b71c4bb578774cb58f7e2f2f074439ff
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2470-1343&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2470-1343&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2470-1343&client=summon