Syn and Anti Metal Complexes of 24π Antiaromatic Bis(Dicarbonylrhodium(I))Dithiaamethyrin.
Isomer
aromaticity
coordination chemistry
porphyrinoids
Journal
Chemistry, an Asian journal
ISSN: 1861-471X
Titre abrégé: Chem Asian J
Pays: Germany
ID NLM: 101294643
Informations de publication
Date de publication:
15 Jul 2022
15 Jul 2022
Historique:
revised:
25
04
2022
received:
28
02
2022
pubmed:
7
5
2022
medline:
7
5
2022
entrez:
6
5
2022
Statut:
ppublish
Résumé
From the reaction of sterically less hindered tetrapropyl[24]dithiaamethyrin(1.0.0.1.0.0) 5, with [Rh(CO)
Identifiants
pubmed: 35514150
doi: 10.1002/asia.202200198
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202200198Informations de copyright
© 2022 Wiley-VCH GmbH.
Références
J. L. Sessler, S. J. Weghorn in Expanded, Contracted & Isomeric Porphyrin, Vol. 16 (Eds.: J. E. Baldwin, P. D. Magnus), Pergamon, Elsevier Science Ltd, New York, USA, 1997.
T. Tanaka, A. Osuka, Chem. Rev. 2017, 117, 2584-2640;
T. Sarma, P. K. Panda, Chem. Rev. 2017, 117, 2785-2838;
J.-i. Setsune, Chem. Rev. 2017, 117, 3044-3101;
T. Chatterjee, A. Srinivasan, M. Ravikanth, T. K. Chandrashekar, Chem. Rev. 2017, 117, 3329-3376 and references cited therein.
B. Szyszko, M. J. Białek, E. Pacholska-Dudziak, L. Latos-Grażyński, Chem. Rev. 2017, 117, 2839-2909 and references cited therein.
Y. M. Sung, J. Oh, W.-Y. Cha, W. Kim, J. M. Lim, M.-C. Yoon, D. Kim, Chem. Rev. 2017, 117, 2257-2312;
J. Mack, Chem. Rev. 2017, 117, 3444-3478 and references cited therein.
J. L. Sessler, A. Gebauer, A. Guba, M. Scherer, V. Lynch, Inorg. Chem. 1998, 37, 2073-2076;
A. K. Burrell, J. L. Sessler, M. J. Cyr, E. McGhee, J. A. Ibers, Angew. Chem. Int. Ed. Engl. 1991, 30, 91-93;
Angew. Chem. 1991, 103, 83-85;
A. Srinivasan, H. Furuta, A. Osuka, Chem. Commun. 2001, 1666-1667;
S. J. Narayanan, B. Sridevi, T. K. Chandrashekar, U. Englich, K. Ruhlandt-Senge, Inorg. Chem. 2001, 40, 1637-1645;
T. Yoneda, H. Mori, B. S. Lee, M.-C. Yoon, D. Kim, A. Osuka, Chem. Commun. 2012, 48, 6785-6787;
J.-i. Setsune, M. Toda, T. Yoshida, K. Imamura, K. Watanabe, Chem. Eur. J. 2015, 21, 12715-12727;
G. Anguera, W.-Y. Cha, M. D. Moore, J. T. Brewster II, M. Y. Zhao, V. D. Lynch, D. Kim, J. L. Sessler, Angew. Chem. Int. Ed. 2018, 57, 2575-2579;
Angew. Chem. 2018, 130, 2605-2609;
S. Samala, R. Dutta, Q. He, Y. Park, B. Chandra, V. M. Lynch, Y. M. Jung, J. L. Sessler, C.-H. Lee, Chem. Commun. 2020, 56, 758-761;
J. T. Brewster II, H. D. Root, H. Zafar, G. D. Thiabaud, A. C. Sedgwick, J. He, V. M. Lynch, J. L. Sessler, Molecules 2020, 25, 1446.
A. Takenaka, Y. Sasada, H. Ogoshi, T. Omura, Z. Yoshida, Acta Crystallogr. Sect. B 1975, 31, 1-6.
Y. Ishimaru, N. Shimoyama, T. Fujihara, K. Watanabe, J.-i. Setsune, Chem. Asian J. 2015, 10, 329-333.
Deposition Number(s)2149677 (6-syn) and CCDC 2149678 (6-anti) contain(s) the supplementary crystallographic data for this paper. These data are provided free of charge by the joint Cambridge Crystallographic Data Centre and Fachinformationszentrum Karlsruhe Access Structures service.