Reduction of Quinones by NADH Catalyzed by Organoiridium Complexes
One electron at a time: Half‐sandwich organometallic cyclopentadienyl–IrIII complexes containing N,N‐chelated ligands can catalyze the reduction of quinones (Q), such as vitamin K3, to semiquinones (Q.−) by coenzyme NADH (see picture). DFT calculations suggest that the mechanism involves hydride tra...
Saved in:
Published in | Angewandte Chemie International Edition Vol. 52; no. 15; pp. 4194 - 4197 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
08.04.2013
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | One electron at a time: Half‐sandwich organometallic cyclopentadienyl–IrIII complexes containing N,N‐chelated ligands can catalyze the reduction of quinones (Q), such as vitamin K3, to semiquinones (Q.−) by coenzyme NADH (see picture). DFT calculations suggest that the mechanism involves hydride transfer followed by two one‐electron transfers and the unusual IrII oxidation state as a key transient intermediate. |
---|---|
AbstractList | One electron at a time: Half-sandwich organometallic cyclopentadienyl-Ir(III) complexes containing N,N-chelated ligands can catalyze the reduction of quinones (Q), such as vitaminK3 , to semiquinones (Q(.-) ) by coenzyme NADH. DFT calculations suggest that the mechanism involves hydride transfer followed by two one-electron transfers and the unusual Ir(II) oxidation state as a key transient intermediate. One electron at a time: Half‐sandwich organometallic cyclopentadienyl–IrIII complexes containing N,N‐chelated ligands can catalyze the reduction of quinones (Q), such as vitamin K3, to semiquinones (Q.−) by coenzyme NADH (see picture). DFT calculations suggest that the mechanism involves hydride transfer followed by two one‐electron transfers and the unusual IrII oxidation state as a key transient intermediate. One electron at a time: Half-sandwich organometallic cyclopentadienyl-Ir super(III) complexes containing N,N-chelated ligands can catalyze the reduction of quinones (Q), such as vitaminK sub(3), to semiquinones (Q super(.-)) by coenzyme NADH (see picture). DFT calculations suggest that the mechanism involves hydride transfer followed by two one-electron transfers and the unusual Ir super(II) oxidation state as a key transient intermediate. |
Author | Liu, Zhe Habtemariam, Abraha Butler, Jennifer S. Sadler, Peter J. Deeth, Robert J. Newton, Mark E. |
Author_xml | – sequence: 1 givenname: Zhe surname: Liu fullname: Liu, Zhe organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 2 givenname: Robert J. surname: Deeth fullname: Deeth, Robert J. organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 3 givenname: Jennifer S. surname: Butler fullname: Butler, Jennifer S. organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 4 givenname: Abraha surname: Habtemariam fullname: Habtemariam, Abraha organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 5 givenname: Mark E. surname: Newton fullname: Newton, Mark E. organization: Department of Physics, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 6 givenname: Peter J. surname: Sadler fullname: Sadler, Peter J. email: p.j.sadler@warwick.ac.uk organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23471835$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkUlv1DAYhi1URBe4ckSRuHDJ4CXeLkjD0FXVdBEIbpYnsYtLYg92Ah1-PY6mHZVKqD3Zsp_n1We_u2DLB28AeI3gBEGI32vvzARDRCDkFX8GdhDFqCSck628rwgpuaBoG-ymdJ15ISB7AbYxqTgShO6Aj5emGereBV8EW1wMbsxPxWJVzKefjoqZ7nW7-mOa8eQsXmkfXHSNG7piFrpla25MegmeW90m8-p23QNfDvY_z47K07PD49n0tKxZhXmJKGKackGapjZVIyxH1C4YR1hqjoWUTDeUW6gZ5tJKbRtC87OwxYRxU2myBz6sc5fDojM5xPdRt2oZXafjSgXt1L833n1XV-GXIoxBLmEOeHcbEMPPwaRedS7Vpm21N2FICnEIpZACPgEluCKCQTKibx-g12GIPv_ESGGGCaQsU2_uD7-Z-q6JDFRroI4hpWisql2vx2LyW1yrEFRj4WosXG0Kz9rkgXaX_F9BroXfrjWrR2g1nR_v33fLtetSb242ro4_FOOEU_V1fqi-nRycnGN2rubkL9YGywc |
CODEN | ACIEAY |
CitedBy_id | crossref_primary_10_1002_ange_202206831 crossref_primary_10_1002_cctc_201601307 crossref_primary_10_1021_ic400835n crossref_primary_10_1002_anie_202312897 crossref_primary_10_3184_003685014X13898980185076 crossref_primary_10_1039_D2DT01055K crossref_primary_10_1016_j_cclet_2021_11_017 crossref_primary_10_1002_aoc_5053 crossref_primary_10_1016_j_ejmech_2015_12_035 crossref_primary_10_1007_s11426_019_9583_4 crossref_primary_10_1002_anie_202403827 crossref_primary_10_1021_acs_inorgchem_7b01959 crossref_primary_10_1039_C9QI01161G crossref_primary_10_1039_D0CC04970K crossref_primary_10_1039_D3DT01696J crossref_primary_10_1016_j_mcat_2022_112521 crossref_primary_10_1007_s00775_018_1578_0 crossref_primary_10_1016_j_molstruc_2024_138405 crossref_primary_10_1021_acs_inorgchem_2c00059 crossref_primary_10_1002_cbic_201900268 crossref_primary_10_1039_C8CY01190G crossref_primary_10_1039_C8DT02963F crossref_primary_10_1021_ar400266c crossref_primary_10_1038_s41467_018_04772_x crossref_primary_10_1002_ange_201311161 crossref_primary_10_1002_anie_201311192 crossref_primary_10_1039_D0DT02408B crossref_primary_10_1021_acs_inorgchem_3c03801 crossref_primary_10_1016_j_poly_2018_05_060 crossref_primary_10_1039_C8QI00476E crossref_primary_10_1021_acsami_1c06381 crossref_primary_10_1038_s41598_017_14728_8 crossref_primary_10_1039_C4CC05313C crossref_primary_10_1021_acs_inorgchem_5b02697 crossref_primary_10_1021_acs_chemrev_8b00493 crossref_primary_10_1039_C7DT00575J crossref_primary_10_3389_fchem_2022_906954 crossref_primary_10_6023_cjoc202404041 crossref_primary_10_1002_chem_201600310 crossref_primary_10_1002_asia_201800103 crossref_primary_10_1016_j_jorganchem_2018_08_006 crossref_primary_10_1021_acs_organomet_8b00402 crossref_primary_10_1021_jacs_6b02470 crossref_primary_10_1021_ol401610e crossref_primary_10_1038_s41557_024_01722_7 crossref_primary_10_1021_acs_inorgchem_8b01944 crossref_primary_10_1039_D3CY01048A crossref_primary_10_1002_asia_201801058 crossref_primary_10_1016_j_ica_2021_120754 crossref_primary_10_1021_cs501874v crossref_primary_10_1039_D0DT01547D crossref_primary_10_1039_D4DT03219E crossref_primary_10_1021_acs_inorgchem_6b01220 crossref_primary_10_1038_s41467_022_29969_z crossref_primary_10_1039_C9QI00081J crossref_primary_10_1002_asia_201801323 crossref_primary_10_1016_j_ccr_2018_02_006 crossref_primary_10_1021_acscatal_6b00395 crossref_primary_10_1021_acscatal_7b02387 crossref_primary_10_1039_D4QI02472A crossref_primary_10_1039_D0CB00150C crossref_primary_10_1002_anie_201311161 crossref_primary_10_1002_ange_201511917 crossref_primary_10_1021_acs_jmedchem_3c01276 crossref_primary_10_1016_j_jinorgbio_2019_110983 crossref_primary_10_1002_ange_201311192 crossref_primary_10_1039_C7CC08270C crossref_primary_10_1002_cctc_202401490 crossref_primary_10_1016_j_jorganchem_2024_123168 crossref_primary_10_1039_C8DT03159B crossref_primary_10_1021_jacs_3c00237 crossref_primary_10_1002_chem_201800504 crossref_primary_10_1002_bkcs_11054 crossref_primary_10_1039_C4CP02255F crossref_primary_10_1039_D0DT00627K crossref_primary_10_1007_s11426_024_2533_4 crossref_primary_10_1016_j_jorganchem_2017_03_038 crossref_primary_10_1039_C8QI00620B crossref_primary_10_1002_ange_202403827 crossref_primary_10_1039_C7DT03265J crossref_primary_10_1016_j_ccr_2018_01_010 crossref_primary_10_1039_D0CC05912A crossref_primary_10_1021_acs_inorgchem_1c02250 crossref_primary_10_1038_ncomms7582 crossref_primary_10_1016_j_jcat_2023_115185 crossref_primary_10_1039_D3RA05412H crossref_primary_10_1021_acs_joc_1c01992 crossref_primary_10_1039_D1DT03080A crossref_primary_10_1016_j_jinorgbio_2017_12_019 crossref_primary_10_1016_j_jinorgbio_2015_10_008 crossref_primary_10_1002_cctc_202000488 crossref_primary_10_1002_ange_202312897 crossref_primary_10_1002_anie_201511917 crossref_primary_10_1002_ejic_201901055 crossref_primary_10_1002_anie_202206831 crossref_primary_10_1002_aoc_4633 crossref_primary_10_1016_j_jorganchem_2019_121087 crossref_primary_10_1021_acs_inorgchem_3c02882 crossref_primary_10_1002_cmdc_202100297 crossref_primary_10_1016_j_jinorgbio_2018_09_009 crossref_primary_10_1021_acs_inorgchem_5b01832 crossref_primary_10_1007_s11244_013_0187_y crossref_primary_10_1021_acs_inorgchem_6b02474 crossref_primary_10_1002_chem_201806351 crossref_primary_10_1021_acs_organomet_5b00097 crossref_primary_10_1021_acsanm_1c02996 crossref_primary_10_1039_D3QI02047A crossref_primary_10_1021_acs_inorgchem_8b02161 crossref_primary_10_1021_acs_jpcc_8b08322 crossref_primary_10_1128_AEM_01758_21 crossref_primary_10_1016_j_jinorgbio_2018_11_011 crossref_primary_10_1016_j_dyepig_2018_10_019 crossref_primary_10_1016_j_jorganchem_2021_121748 crossref_primary_10_1039_D0QI00846J crossref_primary_10_1039_D3DT04361D |
Cites_doi | 10.1002/ange.201102795 10.1039/C0NJ00478B 10.1039/C1CC15378A 10.1002/ejic.200800469 10.1002/anie.201102795 10.1002/cphc.200500640 10.1002/ange.201108175 10.1042/BJ20091382 10.1146/annurev.nu.15.070195.002151 10.1590/S0103-50532011000300002 10.1021/om200251k 10.1016/S0163-7258(02)00327-3 10.1084/jem.20020885 10.1002/ange.200704136 10.1002/anie.201108175 10.1021/bi027158b 10.1021/ja0385179 10.1073/pnas.76.2.954 10.1002/bmc.1130020103 10.1021/bi00398a029 10.1021/jm2000932 10.1099/13500872-145-8-1817 10.1042/BST0330525 10.1002/9783527623075 10.1007/978-3-642-15334-1 10.1016/j.bbabio.2011.05.021 10.1351/pac200880081799 10.1021/ja064708a 10.1054/mehy.2001.1307 10.1002/chem.200900821 10.1021/ar030171j 10.1016/j.jorganchem.2006.10.033 10.1021/ic200607j 10.1002/anie.200704136 10.1016/0005-2728(80)90095-X 10.1021/ic2005248 10.1021/om2005468 10.1093/ajcn/87.4.985 10.1016/j.molcata.2006.02.009 10.1016/S0899-9007(01)00709-2 10.1021/jp060836 10.1039/C2CC37832A 10.1073/pnas.92.19.8846 10.1021/ja00077a070 10.4061/2011/816202 10.1021/om201218j 10.1023/A:1009624111275 |
ContentType | Journal Article |
Copyright | Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim 2013 |
Copyright_xml | – notice: Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim – notice: Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim – notice: Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim 2013 |
DBID | BSCLL 24P AAYXX CITATION CGR CUY CVF ECM EIF NPM 7TM K9. 7X8 7SR 8BQ 8FD JG9 5PM |
DOI | 10.1002/anie.201300747 |
DatabaseName | Istex Wiley Online Library Open Access CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Nucleic Acids Abstracts ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic Engineered Materials Abstracts METADEX Technology Research Database Materials Research Database PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Health & Medical Complete (Alumni) Nucleic Acids Abstracts MEDLINE - Academic Materials Research Database Engineered Materials Abstracts Technology Research Database METADEX |
DatabaseTitleList | ProQuest Health & Medical Complete (Alumni) Materials Research Database |
Database_xml | – sequence: 1 dbid: 24P name: Wiley Online Library Open Access url: https://authorservices.wiley.com/open-science/open-access/browse-journals.html sourceTypes: Publisher – sequence: 2 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 – sequence: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 1521-3773 |
Edition | International ed. in English |
EndPage | 4197 |
ExternalDocumentID | PMC3660790 2933839921 23471835 10_1002_anie_201300747 ANIE201300747 ark_67375_WNG_XJFJP26P_N |
Genre | shortCommunication Research Support, Non-U.S. Gov't Journal Article |
GrantInformation_xml | – fundername: Funded Access – fundername: COST Action – fundername: ERC |
GroupedDBID | --- -DZ -~X .3N .GA .Y3 05W 0R~ 10A 1L6 1OB 1OC 1ZS 23M 31~ 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5RE 5VS 66C 6TJ 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A03 AAESR AAEVG AAHHS AANLZ AAONW AASGY AAXRX AAZKR ABCQN ABCUV ABEML ABIJN ABLJU ABPPZ ABPVW ACAHQ ACBWZ ACCFJ ACCZN ACFBH ACGFS ACIWK ACNCT ACPOU ACPRK ACSCC ACXBN ACXQS ADBBV ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AEQDE AEUQT AEUYR AFBPY AFFNX AFFPM AFGKR AFPWT AFRAH AFZJQ AHBTC AHMBA AITYG AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ATUGU AUFTA AZBYB AZFZN AZVAB B-7 BAFTC BDRZF BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BSCLL BTSUX BY8 CS3 D-E D-F D0L DCZOG DPXWK DR1 DR2 DRFUL DRSTM EBS EJD F00 F01 F04 F5P G-S G.N GNP GODZA H.T H.X HBH HGLYW HHY HHZ HZ~ IX1 J0M JPC KQQ LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES M53 MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG P2P P2W P2X P4D PQQKQ Q.N Q11 QB0 QRW R.K RNS ROL RWI RX1 RYL SUPJJ TN5 UB1 UPT V2E VQA W8V W99 WBFHL WBKPD WH7 WIB WIH WIK WJL WOHZO WQJ WRC WXSBR WYISQ XG1 XPP XSW XV2 YZZ ZZTAW ~IA ~KM ~WT 24P AAHQN AAMNL AANHP AAYCA ACRPL ACYXJ ADNMO AFWVQ ALVPJ AAYXX ABDBF ABJNI AETEA AEYWJ AGQPQ AGYGG CITATION CGR CUY CVF ECM EIF NPM 7TM K9. 7X8 7SR 8BQ 8FD JG9 5PM |
ID | FETCH-LOGICAL-c6427-1516a5783ddce4d8f715fb67129a728996ad57f0a6279f9afd351302f2367e4a3 |
IEDL.DBID | DR2 |
ISSN | 1433-7851 1521-3773 |
IngestDate | Thu Aug 21 18:32:59 EDT 2025 Fri Jul 11 05:45:49 EDT 2025 Fri Jul 11 03:13:51 EDT 2025 Sun Jul 13 05:11:12 EDT 2025 Mon Jul 21 05:50:14 EDT 2025 Tue Jul 01 02:53:12 EDT 2025 Thu Apr 24 23:00:07 EDT 2025 Wed Jan 22 17:03:07 EST 2025 Wed Oct 30 09:55:56 EDT 2024 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 15 |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c6427-1516a5783ddce4d8f715fb67129a728996ad57f0a6279f9afd351302f2367e4a3 |
Notes | We thank the ERC (Award 247450 to P.J.S.), members of COST Action CM1105 for stimulating discussions, and the Magnetic Resonance Centre (Warwick University) for EPR support. Funded Access ArticleID:ANIE201300747 ark:/67375/WNG-XJFJP26P-N ERC COST Action istex:99FC9AED73C74D8FDD2F4757AE98D986D00A63D0 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Supporting information for this article is available on the WWW under http://dx.doi.org/10.1002/anie.201300747. Re-use of this article is permitted in accordance with the Terms and Conditions set out at http://angewandte.org/open. |
OpenAccessLink | https://proxy.k.utb.cz/login?url=https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201300747 |
PMID | 23471835 |
PQID | 1322623056 |
PQPubID | 946352 |
PageCount | 4 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_3660790 proquest_miscellaneous_1700989800 proquest_miscellaneous_1324386030 proquest_journals_1322623056 pubmed_primary_23471835 crossref_citationtrail_10_1002_anie_201300747 crossref_primary_10_1002_anie_201300747 wiley_primary_10_1002_anie_201300747_ANIE201300747 istex_primary_ark_67375_WNG_XJFJP26P_N |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | April 8, 2013 |
PublicationDateYYYYMMDD | 2013-04-08 |
PublicationDate_xml | – month: 04 year: 2013 text: April 8, 2013 day: 08 |
PublicationDecade | 2010 |
PublicationPlace | Weinheim |
PublicationPlace_xml | – name: Weinheim – name: Germany |
PublicationTitle | Angewandte Chemie International Edition |
PublicationTitleAlternate | Angew. Chem. Int. Ed |
PublicationYear | 2013 |
Publisher | WILEY-VCH Verlag WILEY‐VCH Verlag Wiley Subscription Services, Inc |
Publisher_xml | – name: WILEY-VCH Verlag – name: WILEY‐VCH Verlag – name: Wiley Subscription Services, Inc |
References | C. Frontana, Á. Vázquez-Mayagoitia, J. Garza, R. Vargas, I. González, J. Phys. Chem. A 2006, 110, 9411-9419. K. K.-W. Lo, S. P.-Y. Li, K. Y. Zhang, New J. Chem. 2011, 35, 265-287 J. Hirst, Biochem. J. 2010, 425, 327-339. Angew. Chem. Int. Ed. 2008, 47, 1068-1071 A. C. Allison, Med. Hypotheses 2001, 57, 151-155. T. Yagi, A. Matsuno-Yagi, Biochemistry 2003, 42, 2266-2274. P. R. Rich, D. S. Bendall, Biochim. Biophys. Acta Bioenerg. 1980, 592, 506-518. J. Meiners, M. G. Scheibel, M.-H. Lemée-Cailleau, S. A. Mason, M. B. Boeddinghaus, T. F. Fässler, E. Herdtweck, M. M. Khusniyarov, S. Schneider, Angew. Chem. 2011, 123, 8334-8337 Z. Liu, A. Habtemariam, A. M. Pizarro, G. J. Clarkson, P. J. Sadler, Organometallics 2011, 30, 4702-4710 J. Yuasa, S. Yamada, S. Fukuzumi, J. Am. Chem. Soc. 2006, 128, 14938-14948. B. Soballe, R. K. Poole, Microbiology 1999, 145, 1817-1830 J. B. Schenkman, I. Jansson, Pharmacol. Ther. 2003, 97, 139-152 I. Abraham, R. Joshi, P. Pardasani, R. T. Pardasani, J. Braz. Chem. Soc. 2011, 22, 385-421. J. Yuasa, S. Yamada, S. Fukuzumi, Angew. Chem. 2008, 120, 1084-1087 Y. Takahashi, K.-i. Fujita, R. Yamaguchi, Eur. J. Inorg. Chem. 2008, 4360-4368 B. K. Kubata, Z. Kabututu, T. Nozaki, C. J. Munday, S. Fukuzumi, K. Ohkubo, M. Lazarus, T. Maruyama, S. K. Martin, M. Duszenko, Y. Urade, J. Exp. Med. 2002, 196, 1241-1252. Y. Haroon, D. S. Bacon, J. A. Sadowski, Biomed. Chromatogr. 1987, 2, 4-8 P. Weber, Nutrition 2001, 17, 880-887 J. Yuasa, T. Suenobu, S. Fukuzumi, ChemPhysChem 2006, 7, 942-954 Z. Liu, A. Habtemariam, A. M. Pizarro, S. A. Fletcher, A. Kisova, O. Vrana, L. Salassa, P. C. A. Bruijnincx, G. J. Clarkson, V. Brabec, P. J. Sadler, J. Med. Chem. 2011, 54, 3011-3026 N. R. Bachur, S. L. Gordon, M. V. Gee, H. Kon, Proc. Natl. Acad. Sci. USA 1979, 76, 954-957 K. Matsushita, T. Ohnishi, H. R. Kaback, Biochemistry 1987, 26, 7732-7737 X.-Q. Zhu, Y. Yang, M. Zhang, J.-P. Cheng, J. Am. Chem. Soc. 2003, 125, 15298-15299 A. Kastl, A. Wilbuer, A. L. Merkel, L. Feng, P. Di Fazio, M. Ocker, E. Meggers, Chem. Commun. 2012, 48, 1863-1865 J. W. Suttie, Annu. Rev. Nutr. 1995, 15, 399-417. Z. Liu, L. Salassa, A. Habtemariam, A. M. Pizarro, G. J. Clarkson, P. J. Sadler, Inorg. Chem. 2011, 50, 5777-5783 T. Kimura, K. Ishiwata, S. Kuwata, T. Ikariya, Organometallics 2012, 31, 1204-1207 T. S. Teets, T. R. Cook, B. D. McCarthy, D. G. Nocera, Inorg. Chem. 2011, 50, 5223-5233. P. S. Guin, S. Das, P. C. Mandal, Int. J. Electrochem. 2011, 2011, 1-22 S. Schäfer, W. S. Sheldrick, J. Organomet. Chem. 2007, 692, 1300-1309. J. Hirst, Biochem. Soc. Trans. 2005, 33, 525-529 S. P. Saxena, E. D. Israels, L. G. Israels, Apoptosis 2001, 6, 57-68 J. A. Cowan, Pure Appl. Chem. 2008, 80, 1799-1810 L. Hocharoen, J. A. Cowan, Chem. Eur. J. 2009, 15, 8670-8676 L. A. Oro, C. Claver, Iridium Complexes in Organic Synthesis, Wiley, Weinheim, 2008 P. K. Sasmal, C. N. Streu, E. Meggers, Chem. Commun. 2013, 49, 1581-1587 S. Betanzos-Lara, Z. Liu, A. Habtemariam, A. M. Pizarro, B. Qamar, P. J. Sadler, Angew. Chem. 2012, 124, 3963-3966 Angew. Chem. Int. Ed. 2012, 51, 3897-3900. K. Nimptsch, S. Rohrmann, J. Linseisen, Am. J. Clin. Nutr. 2008, 87, 985-992 J. Gȩbicki, A. Marcinek, J. Zielonka, Acc. Chem. Res. 2004, 37, 379-386 D. G. H. Hetterscheid, B. de Bruin, J. Mol. Catal. A 2006, 251, 291-296 C. W. Cheung, K. S. Chan, Organometallics 2011, 30, 4269-4283 R. Li, M. A. Bianchet, P. Talalay, L. M. Amzel, Proc. Natl. Acad. Sci. USA 1995, 92, 8846-8850 P. G. Andersson, Iridium Catalysis, Springer, Berlin, 2011. P. M. Dey, Methods in Plant Biochemistry (Eds.: P. M. Dey, J. B. Harborne), Academic Press, London, 1989. F. Müh, C. Glöckner, J. Hellmich, A. Zouni, Biochim. Biophys. Acta Bioenerg. 2012, 1817, 44-65 A. M. Kuznetsov, J. Ulstrup, Electron transfer in chemistry and biology: an introduction to the theory, Wiley, Chichester, 1999. Angew. Chem. Int. Ed. 2011, 50, 8184-8187 S. Fukuzumi, T. Okamoto, J. Am. Chem. Soc. 1993, 115, 11600-11601. 1987; 2 1995; 92 2013; 49 2011 1995; 15 2010; 425 2002; 196 2006; 7 2006; 251 2008 2011; 30 2006; 110 2011; 54 2011; 35 2011 2011; 123 50 1999; 145 1980; 592 1979; 76 2003; 97 2012; 31 1999 2011; 2011 2001; 6 2004; 37 2011; 50 2007; 692 2011; 22 2008; 87 2012 2012; 124 51 2001; 17 2012; 1817 2012; 48 2003; 125 2001; 57 1993; 115 2008 2008; 120 47 2006; 128 2005; 33 2003; 42 2008; 80 2009; 15 1989 1987; 26 e_1_2_2_24_2 e_1_2_2_47_2 e_1_2_2_4_2 e_1_2_2_22_2 e_1_2_2_49_2 e_1_2_2_6_2 e_1_2_2_20_2 e_1_2_2_2_2 e_1_2_2_41_2 e_1_2_2_8_2 e_1_2_2_28_2 e_1_2_2_43_2 e_1_2_2_43_3 e_1_2_2_26_2 e_1_2_2_45_2 e_1_2_2_13_2 e_1_2_2_36_2 e_1_2_2_11_2 e_1_2_2_38_2 e_1_2_2_51_2 e_1_2_2_19_2 e_1_2_2_30_2 e_1_2_2_53_2 e_1_2_2_30_3 e_1_2_2_51_3 e_1_2_2_17_2 e_1_2_2_32_2 e_1_2_2_55_2 e_1_2_2_15_2 e_1_2_2_34_2 Kuznetsov A. M. (e_1_2_2_57_2) 1999 Dey P. M. (e_1_2_2_1_2) 1989 e_1_2_2_3_2 e_1_2_2_23_2 e_1_2_2_48_2 e_1_2_2_5_2 e_1_2_2_21_2 e_1_2_2_40_2 e_1_2_2_29_2 e_1_2_2_42_2 e_1_2_2_7_2 e_1_2_2_27_2 e_1_2_2_44_2 e_1_2_2_9_2 e_1_2_2_25_2 e_1_2_2_46_2 e_1_2_2_12_2 e_1_2_2_37_2 e_1_2_2_10_2 e_1_2_2_39_2 e_1_2_2_50_2 e_1_2_2_18_2 e_1_2_2_31_2 e_1_2_2_52_2 e_1_2_2_16_2 e_1_2_2_33_2 e_1_2_2_54_2 e_1_2_2_14_2 e_1_2_2_35_2 e_1_2_2_56_2 18165966 - Angew Chem Int Ed Engl. 2008;47(6):1068-71 8527227 - Annu Rev Nutr. 1995;15:399-417 16869691 - J Phys Chem A. 2006 Aug 3;110(30):9411-9 21744449 - Angew Chem Int Ed Engl. 2011 Aug 22;50(35):8184-7 21679684 - Biochim Biophys Acta. 2012 Jan;1817(1):44-65 12559387 - Pharmacol Ther. 2003 Feb;97(2):139-52 34156 - Proc Natl Acad Sci U S A. 1979 Feb;76(2):954-7 6251868 - Biochim Biophys Acta. 1980 Oct 3;592(3):506-18 16521156 - Chemphyschem. 2006 Apr 10;7(4):942-54 15916556 - Biochem Soc Trans. 2005 Jun;33(Pt 3):525-9 3508094 - Biomed Chromatogr. 1987 Feb;2(1):4-8 10463148 - Microbiology. 1999 Aug;145 ( Pt 8):1817-30 11684396 - Nutrition. 2001 Oct;17(10):880-7 12600193 - Biochemistry. 2003 Mar 4;42(8):2266-74 21443199 - J Med Chem. 2011 Apr 28;54(8):3011-26 14664567 - J Am Chem Soc. 2003 Dec 17;125(50):15298-9 21557564 - Inorg Chem. 2011 Jun 6;50(11):5223-33 22057186 - Chem Commun (Camb). 2012 Feb 11;48(13):1863-5 18400723 - Am J Clin Nutr. 2008 Apr;87(4):985-92 15196047 - Acc Chem Res. 2004 Jun;37(6):379-86 17105305 - J Am Chem Soc. 2006 Nov 22;128(46):14938-48 20025615 - Biochem J. 2010 Jan 15;425(2):327-39 22415924 - Angew Chem Int Ed Engl. 2012 Apr 16;51(16):3897-900 7568029 - Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8846-50 21618978 - Inorg Chem. 2011 Jun 20;50(12):5777-83 19685535 - Chemistry. 2009 Sep 7;15(35):8670-6 11461163 - Med Hypotheses. 2001 Aug;57(2):151-5 3122832 - Biochemistry. 1987 Dec 1;26(24):7732-7 12417633 - J Exp Med. 2002 Nov 4;196(9):1241-51 23250079 - Chem Commun (Camb). 2013 Feb 25;49(16):1581-7 11321042 - Apoptosis. 2001 Feb-Apr;6(1-2):57-68 |
References_xml | – reference: J. Yuasa, S. Yamada, S. Fukuzumi, J. Am. Chem. Soc. 2006, 128, 14938-14948. – reference: C. W. Cheung, K. S. Chan, Organometallics 2011, 30, 4269-4283; – reference: P. S. Guin, S. Das, P. C. Mandal, Int. J. Electrochem. 2011, 2011, 1-22; – reference: N. R. Bachur, S. L. Gordon, M. V. Gee, H. Kon, Proc. Natl. Acad. Sci. USA 1979, 76, 954-957; – reference: B. Soballe, R. K. Poole, Microbiology 1999, 145, 1817-1830; – reference: F. Müh, C. Glöckner, J. Hellmich, A. Zouni, Biochim. Biophys. Acta Bioenerg. 2012, 1817, 44-65; – reference: Z. Liu, A. Habtemariam, A. M. Pizarro, S. A. Fletcher, A. Kisova, O. Vrana, L. Salassa, P. C. A. Bruijnincx, G. J. Clarkson, V. Brabec, P. J. Sadler, J. Med. Chem. 2011, 54, 3011-3026; – reference: T. Kimura, K. Ishiwata, S. Kuwata, T. Ikariya, Organometallics 2012, 31, 1204-1207; – reference: J. Meiners, M. G. Scheibel, M.-H. Lemée-Cailleau, S. A. Mason, M. B. Boeddinghaus, T. F. Fässler, E. Herdtweck, M. M. Khusniyarov, S. Schneider, Angew. Chem. 2011, 123, 8334-8337; – reference: A. Kastl, A. Wilbuer, A. L. Merkel, L. Feng, P. Di Fazio, M. Ocker, E. Meggers, Chem. Commun. 2012, 48, 1863-1865; – reference: Angew. Chem. Int. Ed. 2008, 47, 1068-1071; – reference: S. Fukuzumi, T. Okamoto, J. Am. Chem. Soc. 1993, 115, 11600-11601. – reference: J. A. Cowan, Pure Appl. Chem. 2008, 80, 1799-1810; – reference: C. Frontana, Á. Vázquez-Mayagoitia, J. Garza, R. Vargas, I. González, J. Phys. Chem. A 2006, 110, 9411-9419. – reference: D. G. H. Hetterscheid, B. de Bruin, J. Mol. Catal. A 2006, 251, 291-296; – reference: L. Hocharoen, J. A. Cowan, Chem. Eur. J. 2009, 15, 8670-8676; – reference: R. Li, M. A. Bianchet, P. Talalay, L. M. Amzel, Proc. Natl. Acad. Sci. USA 1995, 92, 8846-8850; – reference: A. C. Allison, Med. Hypotheses 2001, 57, 151-155. – reference: Z. Liu, A. Habtemariam, A. M. Pizarro, G. J. Clarkson, P. J. Sadler, Organometallics 2011, 30, 4702-4710; – reference: P. K. Sasmal, C. N. Streu, E. Meggers, Chem. Commun. 2013, 49, 1581-1587; – reference: K. Matsushita, T. Ohnishi, H. R. Kaback, Biochemistry 1987, 26, 7732-7737; – reference: S. Betanzos-Lara, Z. Liu, A. Habtemariam, A. M. Pizarro, B. Qamar, P. J. Sadler, Angew. Chem. 2012, 124, 3963-3966; – reference: J. Hirst, Biochem. J. 2010, 425, 327-339. – reference: B. K. Kubata, Z. Kabututu, T. Nozaki, C. J. Munday, S. Fukuzumi, K. Ohkubo, M. Lazarus, T. Maruyama, S. K. Martin, M. Duszenko, Y. Urade, J. Exp. Med. 2002, 196, 1241-1252. – reference: A. M. Kuznetsov, J. Ulstrup, Electron transfer in chemistry and biology: an introduction to the theory, Wiley, Chichester, 1999. – reference: P. M. Dey, Methods in Plant Biochemistry (Eds.: P. M. Dey, J. B. Harborne), Academic Press, London, 1989. – reference: X.-Q. Zhu, Y. Yang, M. Zhang, J.-P. Cheng, J. Am. Chem. Soc. 2003, 125, 15298-15299; – reference: J. Yuasa, T. Suenobu, S. Fukuzumi, ChemPhysChem 2006, 7, 942-954; – reference: S. Schäfer, W. S. Sheldrick, J. Organomet. Chem. 2007, 692, 1300-1309. – reference: T. S. Teets, T. R. Cook, B. D. McCarthy, D. G. Nocera, Inorg. Chem. 2011, 50, 5223-5233. – reference: Y. Takahashi, K.-i. Fujita, R. Yamaguchi, Eur. J. Inorg. Chem. 2008, 4360-4368; – reference: P. R. Rich, D. S. Bendall, Biochim. Biophys. Acta Bioenerg. 1980, 592, 506-518. – reference: P. G. Andersson, Iridium Catalysis, Springer, Berlin, 2011. – reference: J. Gȩbicki, A. Marcinek, J. Zielonka, Acc. Chem. Res. 2004, 37, 379-386; – reference: P. Weber, Nutrition 2001, 17, 880-887; – reference: L. A. Oro, C. Claver, Iridium Complexes in Organic Synthesis, Wiley, Weinheim, 2008; – reference: K. Nimptsch, S. Rohrmann, J. Linseisen, Am. J. Clin. Nutr. 2008, 87, 985-992; – reference: J. B. Schenkman, I. Jansson, Pharmacol. Ther. 2003, 97, 139-152; – reference: S. P. Saxena, E. D. Israels, L. G. Israels, Apoptosis 2001, 6, 57-68; – reference: J. Hirst, Biochem. Soc. Trans. 2005, 33, 525-529; – reference: J. W. Suttie, Annu. Rev. Nutr. 1995, 15, 399-417. – reference: Y. Haroon, D. S. Bacon, J. A. Sadowski, Biomed. Chromatogr. 1987, 2, 4-8; – reference: J. Yuasa, S. Yamada, S. Fukuzumi, Angew. Chem. 2008, 120, 1084-1087; – reference: Angew. Chem. Int. Ed. 2011, 50, 8184-8187; – reference: I. Abraham, R. Joshi, P. Pardasani, R. T. Pardasani, J. Braz. Chem. Soc. 2011, 22, 385-421. – reference: Angew. Chem. Int. Ed. 2012, 51, 3897-3900. – reference: T. Yagi, A. Matsuno-Yagi, Biochemistry 2003, 42, 2266-2274. – reference: Z. Liu, L. Salassa, A. Habtemariam, A. M. Pizarro, G. J. Clarkson, P. J. Sadler, Inorg. Chem. 2011, 50, 5777-5783; – reference: K. K.-W. Lo, S. P.-Y. Li, K. Y. Zhang, New J. Chem. 2011, 35, 265-287; – year: 2011 – volume: 592 start-page: 506 year: 1980 end-page: 518 publication-title: Biochim. Biophys. Acta Bioenerg. – volume: 50 start-page: 5777 year: 2011 end-page: 5783 publication-title: Inorg. Chem. – volume: 120 47 start-page: 1084 1068 year: 2008 2008 end-page: 1087 1071 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 1817 start-page: 44 year: 2012 end-page: 65 publication-title: Biochim. Biophys. Acta Bioenerg. – volume: 124 51 start-page: 3963 3897 year: 2012 2012 end-page: 3966 3900 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 115 start-page: 11600 year: 1993 end-page: 11601 publication-title: J. Am. Chem. Soc. – volume: 196 start-page: 1241 year: 2002 end-page: 1252 publication-title: J. Exp. Med. – volume: 97 start-page: 139 year: 2003 end-page: 152 publication-title: Pharmacol. Ther. – volume: 425 start-page: 327 year: 2010 end-page: 339 publication-title: Biochem. J. – volume: 2 start-page: 4 year: 1987 end-page: 8 publication-title: Biomed. Chromatogr. – volume: 26 start-page: 7732 year: 1987 end-page: 7737 publication-title: Biochemistry – volume: 92 start-page: 8846 year: 1995 end-page: 8850 publication-title: Proc. Natl. Acad. Sci. USA – year: 1989 – volume: 50 start-page: 5223 year: 2011 end-page: 5233 publication-title: Inorg. Chem. – volume: 48 start-page: 1863 year: 2012 end-page: 1865 publication-title: Chem. Commun. – volume: 123 50 start-page: 8334 8184 year: 2011 2011 end-page: 8337 8187 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 6 start-page: 57 year: 2001 end-page: 68 publication-title: Apoptosis – volume: 125 start-page: 15298 year: 2003 end-page: 15299 publication-title: J. Am. Chem. Soc. – volume: 33 start-page: 525 year: 2005 end-page: 529 publication-title: Biochem. Soc. Trans. – volume: 7 start-page: 942 year: 2006 end-page: 954 publication-title: ChemPhysChem – volume: 35 start-page: 265 year: 2011 end-page: 287 publication-title: New J. Chem. – volume: 128 start-page: 14938 year: 2006 end-page: 14948 publication-title: J. Am. Chem. Soc. – volume: 54 start-page: 3011 year: 2011 end-page: 3026 publication-title: J. Med. Chem. – volume: 87 start-page: 985 year: 2008 end-page: 992 publication-title: Am. J. Clin. Nutr. – volume: 2011 start-page: 1 year: 2011 end-page: 22 publication-title: Int. J. Electrochem. – volume: 22 start-page: 385 year: 2011 end-page: 421 publication-title: J. Braz. Chem. Soc. – volume: 57 start-page: 151 year: 2001 end-page: 155 publication-title: Med. Hypotheses – volume: 31 start-page: 1204 year: 2012 end-page: 1207 publication-title: Organometallics – volume: 251 start-page: 291 year: 2006 end-page: 296 publication-title: J. Mol. Catal. A – volume: 49 start-page: 1581 year: 2013 end-page: 1587 publication-title: Chem. Commun. – volume: 15 start-page: 8670 year: 2009 end-page: 8676 publication-title: Chem. Eur. J. – volume: 110 start-page: 9411 year: 2006 end-page: 9419 publication-title: J. Phys. Chem. A – volume: 30 start-page: 4702 year: 2011 end-page: 4710 publication-title: Organometallics – volume: 80 start-page: 1799 year: 2008 end-page: 1810 publication-title: Pure Appl. Chem. – year: 2008 – volume: 15 start-page: 399 year: 1995 end-page: 417 publication-title: Annu. Rev. Nutr. – volume: 76 start-page: 954 year: 1979 end-page: 957 publication-title: Proc. Natl. Acad. Sci. USA – volume: 30 start-page: 4269 year: 2011 end-page: 4283 publication-title: Organometallics – volume: 17 start-page: 880 year: 2001 end-page: 887 publication-title: Nutrition – volume: 42 start-page: 2266 year: 2003 end-page: 2274 publication-title: Biochemistry – volume: 37 start-page: 379 year: 2004 end-page: 386 publication-title: Acc. Chem. Res. – volume: 692 start-page: 1300 year: 2007 end-page: 1309 publication-title: J. Organomet. Chem. – volume: 145 start-page: 1817 year: 1999 end-page: 1830 publication-title: Microbiology – start-page: 4360 year: 2008 end-page: 4368 publication-title: Eur. J. Inorg. Chem. – year: 1999 – ident: e_1_2_2_51_2 doi: 10.1002/ange.201102795 – ident: e_1_2_2_28_2 doi: 10.1039/C0NJ00478B – ident: e_1_2_2_53_2 – ident: e_1_2_2_27_2 doi: 10.1039/C1CC15378A – ident: e_1_2_2_50_2 doi: 10.1002/ejic.200800469 – ident: e_1_2_2_51_3 doi: 10.1002/anie.201102795 – volume-title: Methods in Plant Biochemistry year: 1989 ident: e_1_2_2_1_2 – ident: e_1_2_2_18_2 doi: 10.1002/cphc.200500640 – ident: e_1_2_2_2_2 – ident: e_1_2_2_30_2 doi: 10.1002/ange.201108175 – ident: e_1_2_2_11_2 doi: 10.1042/BJ20091382 – ident: e_1_2_2_33_2 doi: 10.1146/annurev.nu.15.070195.002151 – ident: e_1_2_2_46_2 – ident: e_1_2_2_16_2 doi: 10.1590/S0103-50532011000300002 – ident: e_1_2_2_40_2 – ident: e_1_2_2_48_2 doi: 10.1021/om200251k – ident: e_1_2_2_8_2 doi: 10.1016/S0163-7258(02)00327-3 – ident: e_1_2_2_38_2 doi: 10.1084/jem.20020885 – ident: e_1_2_2_43_2 doi: 10.1002/ange.200704136 – ident: e_1_2_2_30_3 doi: 10.1002/anie.201108175 – ident: e_1_2_2_5_2 doi: 10.1021/bi027158b – ident: e_1_2_2_42_2 doi: 10.1021/ja0385179 – ident: e_1_2_2_9_2 doi: 10.1073/pnas.76.2.954 – ident: e_1_2_2_15_2 doi: 10.1002/bmc.1130020103 – ident: e_1_2_2_7_2 doi: 10.1021/bi00398a029 – ident: e_1_2_2_24_2 doi: 10.1021/jm2000932 – ident: e_1_2_2_3_2 doi: 10.1099/13500872-145-8-1817 – ident: e_1_2_2_4_2 doi: 10.1042/BST0330525 – ident: e_1_2_2_21_2 doi: 10.1002/9783527623075 – ident: e_1_2_2_22_2 doi: 10.1007/978-3-642-15334-1 – ident: e_1_2_2_14_2 doi: 10.1016/j.bbabio.2011.05.021 – ident: e_1_2_2_55_2 doi: 10.1351/pac200880081799 – ident: e_1_2_2_17_2 – ident: e_1_2_2_44_2 doi: 10.1021/ja064708a – ident: e_1_2_2_37_2 doi: 10.1054/mehy.2001.1307 – ident: e_1_2_2_56_2 doi: 10.1002/chem.200900821 – ident: e_1_2_2_41_2 doi: 10.1021/ar030171j – ident: e_1_2_2_6_2 – ident: e_1_2_2_29_2 doi: 10.1016/j.jorganchem.2006.10.033 – ident: e_1_2_2_26_2 doi: 10.1021/ic200607j – ident: e_1_2_2_43_3 doi: 10.1002/anie.200704136 – ident: e_1_2_2_45_2 doi: 10.1016/0005-2728(80)90095-X – ident: e_1_2_2_52_2 doi: 10.1021/ic2005248 – ident: e_1_2_2_12_2 – ident: e_1_2_2_25_2 doi: 10.1021/om2005468 – ident: e_1_2_2_36_2 doi: 10.1093/ajcn/87.4.985 – ident: e_1_2_2_47_2 doi: 10.1016/j.molcata.2006.02.009 – ident: e_1_2_2_34_2 – ident: e_1_2_2_32_2 doi: 10.1016/S0899-9007(01)00709-2 – ident: e_1_2_2_31_2 – volume-title: Electron transfer in chemistry and biology: an introduction to the theory year: 1999 ident: e_1_2_2_57_2 – ident: e_1_2_2_39_2 doi: 10.1021/jp060836 – ident: e_1_2_2_54_2 doi: 10.1039/C2CC37832A – ident: e_1_2_2_20_2 – ident: e_1_2_2_10_2 doi: 10.1073/pnas.92.19.8846 – ident: e_1_2_2_19_2 doi: 10.1021/ja00077a070 – ident: e_1_2_2_23_2 – ident: e_1_2_2_13_2 doi: 10.4061/2011/816202 – ident: e_1_2_2_49_2 doi: 10.1021/om201218j – ident: e_1_2_2_35_2 doi: 10.1023/A:1009624111275 – reference: 20025615 - Biochem J. 2010 Jan 15;425(2):327-39 – reference: 16521156 - Chemphyschem. 2006 Apr 10;7(4):942-54 – reference: 15916556 - Biochem Soc Trans. 2005 Jun;33(Pt 3):525-9 – reference: 3508094 - Biomed Chromatogr. 1987 Feb;2(1):4-8 – reference: 11321042 - Apoptosis. 2001 Feb-Apr;6(1-2):57-68 – reference: 21744449 - Angew Chem Int Ed Engl. 2011 Aug 22;50(35):8184-7 – reference: 15196047 - Acc Chem Res. 2004 Jun;37(6):379-86 – reference: 19685535 - Chemistry. 2009 Sep 7;15(35):8670-6 – reference: 21618978 - Inorg Chem. 2011 Jun 20;50(12):5777-83 – reference: 17105305 - J Am Chem Soc. 2006 Nov 22;128(46):14938-48 – reference: 12417633 - J Exp Med. 2002 Nov 4;196(9):1241-51 – reference: 23250079 - Chem Commun (Camb). 2013 Feb 25;49(16):1581-7 – reference: 12600193 - Biochemistry. 2003 Mar 4;42(8):2266-74 – reference: 6251868 - Biochim Biophys Acta. 1980 Oct 3;592(3):506-18 – reference: 22415924 - Angew Chem Int Ed Engl. 2012 Apr 16;51(16):3897-900 – reference: 18400723 - Am J Clin Nutr. 2008 Apr;87(4):985-92 – reference: 18165966 - Angew Chem Int Ed Engl. 2008;47(6):1068-71 – reference: 16869691 - J Phys Chem A. 2006 Aug 3;110(30):9411-9 – reference: 7568029 - Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8846-50 – reference: 12559387 - Pharmacol Ther. 2003 Feb;97(2):139-52 – reference: 21443199 - J Med Chem. 2011 Apr 28;54(8):3011-26 – reference: 34156 - Proc Natl Acad Sci U S A. 1979 Feb;76(2):954-7 – reference: 14664567 - J Am Chem Soc. 2003 Dec 17;125(50):15298-9 – reference: 3122832 - Biochemistry. 1987 Dec 1;26(24):7732-7 – reference: 11461163 - Med Hypotheses. 2001 Aug;57(2):151-5 – reference: 21679684 - Biochim Biophys Acta. 2012 Jan;1817(1):44-65 – reference: 8527227 - Annu Rev Nutr. 1995;15:399-417 – reference: 22057186 - Chem Commun (Camb). 2012 Feb 11;48(13):1863-5 – reference: 11684396 - Nutrition. 2001 Oct;17(10):880-7 – reference: 10463148 - Microbiology. 1999 Aug;145 ( Pt 8):1817-30 – reference: 21557564 - Inorg Chem. 2011 Jun 6;50(11):5223-33 |
SSID | ssj0028806 |
Score | 2.4418273 |
Snippet | One electron at a time: Half‐sandwich organometallic cyclopentadienyl–IrIII complexes containing N,N‐chelated ligands can catalyze the reduction of quinones... One electron at a time: Half-sandwich organometallic cyclopentadienyl-Ir(III) complexes containing N,N-chelated ligands can catalyze the reduction of quinones... One electron at a time: Half-sandwich organometallic cyclopentadienyl-Ir super(III) complexes containing N,N-chelated ligands can catalyze the reduction of... |
SourceID | pubmedcentral proquest pubmed crossref wiley istex |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 4194 |
SubjectTerms | Catalysis Communications hydride transfer Hydrides iridium Iridium - chemistry Ligands Mathematical analysis Metalorganic compounds Molecular Structure NAD - chemistry NADH Organometallic Compounds - chemistry Oxidation-Reduction Quinones Quinones - chemistry radical reactions Reduction Valence |
Title | Reduction of Quinones by NADH Catalyzed by Organoiridium Complexes |
URI | https://api.istex.fr/ark:/67375/WNG-XJFJP26P-N/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201300747 https://www.ncbi.nlm.nih.gov/pubmed/23471835 https://www.proquest.com/docview/1322623056 https://www.proquest.com/docview/1324386030 https://www.proquest.com/docview/1700989800 https://pubmed.ncbi.nlm.nih.gov/PMC3660790 |
Volume | 52 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3db9MwED_BeIAXvhmBMQUJwVO2JHbs5LGUlVKJqExM9M2yHVtEGy1qG2nbX4_PacLKpwSPSc5Rcr67_Bzf_Q7gRZJpTPfTUawlkmpnNFKK6IjrxCY6tzLJsHb4fcnGJ3Qyy2ZXqvhbfoj-hxt6ho_X6OBSrQ6_k4ZiBTamZhHPAe-CMCZsISo67vmjUmecbXkRIRF2oe9YG-P0cHv41lfpBir4_FeQ8-fMyauI1n-SRndAdi_TZqKcHjRrdaAvf-B5_J-3vQu3N3g1HLQGdg-umfl9uDns2sQ9gNfHSP6K0xsubPihqefI_h-qi7AcvBmHQ_w9dHFpKjzjCz8X9bKu6uZLiKHozJyb1UM4GR19HI6jTWOGSLvlCo8cSmDSuTqpnCJolVueZFYx7rCD5LiCY7LKuI0lS3lhC2krkuEGqUW6OEMleQQ7-DCPIWQaw4JiNpeFW-oVStM8MdYWmhJjqAog6iZG6A1rOTbPOBMt33IqUDOi10wAr3r5ry1fx28lX_p57sXk8hSz3HgmPpVvxWwymkxTNhVlAHudIYiNg68ELuIdcnTwMYDn_WWnetxvkXOzaLwMJTlzYfQPMhwZXQsH2wPYbW2rf6CUIHIgWQB8y-p6AaQG374yrz97inDCWMwLd8_UG9VfVCEG5buj_ujJvwx6CrdS3yiERnG-BzvrZWOeObi2VvtwPaXTfe-Y3wDEUjZJ |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V1Jb9QwFH4q7aFc2JdAgSCxnNImcWInBw7DTIeZaRuVqlXnZhzHVqO2M2gW0em_4q_wi_DLBsMqIfXAMfGL5dhvs_3e9wBeeKHEcD_puFIgqHYYOGlKpMOkpz0ZaeGFmDu8l9DeUTAYhsMV-FznwpT4EM2BG0pGoa9RwPFAeusbaiimYGNsFilA4Ku4yh21-GR2bdM3_Y5Z4pe-390-bPecqrCAI427zRxj5agwrEqyTKogizTzQp1SZmyfYLgDoSILmXYF9VmsY6EzEuIFn0a4MxUIYvq9BmtYRhzh-jsHDWKVb8ShTGgixMG69zVOpOtvLY93yQ6u4ZJe_MrJ_TlW83sfujCC3ZvwpZ6-MvbldHM-Szfl5Q_Ikv_V_N6CG5VLbrdKGboNK2p0B9bbdSW8u_D2APFtkYPtsbbfz_MRFjiw04WdtDo9u40nYItLleGbIrd1nE_yLJ-f26htz9SFmt6Doyv5hfuwioN5CDaVqPlSqiMRm91snMog8pTWsQyIUkFqgVNzApcVMDvWBznjJaS0z3EleLMSFrxu6D-WkCS_pXxVMFZDJianGMjHQn6cvOPDQXew79N9nliwUXMer3TYlOM5hXGOjYdswfOm2Uw9XimJkRrPC5qARNRYij_QMAStjc3OxIIHJTM3A_IJOkcktIAtsXlDgOjnyy2j_KRAQSeUuiw2ffoFF_9lKngr6W83T4_-5aNnsN473Nvlu_1k5zFc94u6KIHjRhuwOpvM1RPjnc7Sp4U-sOHDVQvIV4takVA |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwED-NTQJeEN8EBgSJj6doSezYyQMPpV1pO4gKYqJvxnFsLdpop3YVK38VfyI-Jw1UfElIe0xyiaw7n_27-O53AE-jRGG6nwpCJZFUO6FBURAVcBWZSKVGRgnWDr_N2eCQjibJZAu-rWthan6I9ocbeoZbr9HBT0uz94M0FCuwMTWLOA74Jq3yQK--2KBt8XLYsxZ-Fsf9_Q_dQdD0FQiURds8sJsck3amkrJUmpap4VFiCsbt1ic5BiBMlgk3oWQxz0wmTUkSPN8zyHamqST2u5dgB08YMYkspuM2xLPeUNczERJg2_s1TWQY722Od2Mb3EGLnv8O4_6aqvkzhHZ7YP86XGvAq9-pZ9sN2NLTm3Clu-4ZdwtevUcmWLS1PzP-u2U1xVYAfrHy805v4HfxX9Hqqy7xjqsCnVXzqqyWn31cl070uV7chsML0eYd2MbB3AOfKVwjCmZSmdm4LysUTSNtTKYo0ZoWHgRrpQnVUJhjJ40TUZMvxwKVLFole_CilT-tyTv-KPnc2aAVk_NjTHnjifiYvxaTUX80jtlY5B7sro0kGm9fCIzoLYy0WNKDJ-1jq3o8fJFTPVs6GUpSZtfUv8hwpHfNLIb34G5t93ZAMUEYQRIP-MaMaAWQJ3zzybQ6cnzhhLGQZ_absZs7_1CF6OTD_fbq_v-89Bguj3t98WaYHzyAq7FrIEKDMN2F7bP5Uj-0MO6seOQ8x4dPF-2q3wHoFk9Q |
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=Reduction+of+Quinones+by+NADH+Catalyzed+by+Organoiridium+Complexes&rft.jtitle=Angewandte+Chemie+International+Edition&rft.au=Liu%2C+Zhe&rft.au=Deeth%2C+Robert+J.&rft.au=Butler%2C+Jennifer+S.&rft.au=Habtemariam%2C+Abraha&rft.date=2013-04-08&rft.pub=WILEY%E2%80%90VCH+Verlag&rft.issn=1433-7851&rft.eissn=1521-3773&rft.volume=52&rft.issue=15&rft.spage=4194&rft.epage=4197&rft_id=info:doi/10.1002%2Fanie.201300747&rft.externalDBID=10.1002%252Fanie.201300747&rft.externalDocID=ANIE201300747 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1433-7851&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1433-7851&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1433-7851&client=summon |