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Unexpected Product of the Reaction of Iron(II) Dichloroclathrochelate with the [Fe2(μ-S)2(CO)6]2– Cluster Dianion : Synthesis and X-ray Diffraction Structure of the First Cage Complex with Thiol Groups Inherently Bonded to a Macrobicyclic Framework. / Ogienko, M. A.; Konchenko, S. N.; Burdukov, A. B. et al.

In: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, Vol. 44, No. 8, 01.08.2018, p. 496-501.

Research output: Contribution to journal › Article › peer-review

Harvard

Ogienko, MA, Konchenko, SN, Burdukov, AB, Vologzhanina, AV, Lebed, EG & Voloshin, YZ 2018, 'Unexpected Product of the Reaction of Iron(II) Dichloroclathrochelate with the [Fe2(μ-S)2(CO)6]2– Cluster Dianion: Synthesis and X-ray Diffraction Structure of the First Cage Complex with Thiol Groups Inherently Bonded to a Macrobicyclic Framework', Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, vol. 44, no. 8, pp. 496-501. https://doi.org/10.1134/S1070328418080055

APA

Ogienko, M. A., Konchenko, S. N., Burdukov, A. B., Vologzhanina, A. V., Lebed, E. G., & Voloshin, Y. Z. (2018). Unexpected Product of the Reaction of Iron(II) Dichloroclathrochelate with the [Fe2(μ-S)2(CO)6]2– Cluster Dianion: Synthesis and X-ray Diffraction Structure of the First Cage Complex with Thiol Groups Inherently Bonded to a Macrobicyclic Framework. Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 44(8), 496-501. https://doi.org/10.1134/S1070328418080055

Vancouver

Ogienko MA, Konchenko SN, Burdukov AB, Vologzhanina AV, Lebed EG, Voloshin YZ. Unexpected Product of the Reaction of Iron(II) Dichloroclathrochelate with the [Fe2(μ-S)2(CO)6]2– Cluster Dianion: Synthesis and X-ray Diffraction Structure of the First Cage Complex with Thiol Groups Inherently Bonded to a Macrobicyclic Framework. Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2018 Aug 1;44(8):496-501. doi: 10.1134/S1070328418080055

Author

Ogienko, M. A. ; Konchenko, S. N. ; Burdukov, A. B. et al. / Unexpected Product of the Reaction of Iron(II) Dichloroclathrochelate with the [Fe2(μ-S)2(CO)6]2– Cluster Dianion : Synthesis and X-ray Diffraction Structure of the First Cage Complex with Thiol Groups Inherently Bonded to a Macrobicyclic Framework. In: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2018 ; Vol. 44, No. 8. pp. 496-501.

BibTeX

@article{be3209bea39647e7b72a7612dd670601,
title = "Unexpected Product of the Reaction of Iron(II) Dichloroclathrochelate with the [Fe2(μ-S)2(CO)6]2– Cluster Dianion: Synthesis and X-ray Diffraction Structure of the First Cage Complex with Thiol Groups Inherently Bonded to a Macrobicyclic Framework",
abstract = "An attempt to prepare a hybrid clusteroclathrochelate by nucleophilic substitution of iron(II) dichloroclathrochelate by substitution of its chlorine atoms with the [Fe2(μ-S)2(CO)6]2– cluster dianion as a nucleophilic agent generated in situ by the reduction of Fe2(μ-S2)(CO)6 with lithium triethylborohydride unexpectedly gave the macrobicyclic complex with two inherent thiol groups as the single clathrochelate product. Obviously, the initial iron-sulfide cluster underwent a complete decomposition during the reaction, thus acting only as a source of HS– and S2– anions. The composition and the structure of the complex obtained were confirmed by elemental analysis, MALDI-TOF mass spectrometry, 1H and 13C{1H} NMR spectroscopy, and single crystal X-ray diffraction (CIF file CCDC 1585112). The encapsulated iron(II) ion is located at the centre of its FeN6 coordination polyhedron possessing the geometry intermediate between a trigonal prism (the distortion angle φ = 0°) and a trigonal antiprism (φ = 60°) with φ ≈ 25°; the height of this polyhedron is 2.33 {\AA}. The presence of two thiol groups in the vicinal positions of the same ribbed moiety of the macrobicyclic molecule substantially affects the crystal packing of the molecular crystal containing clathrochelate dimers formed by four hydrogen bonds of two types (i.e., two S–H···O and two S–H···N bonds). The obtained cage complex and its deprotonated forms seem to be promising cis-disulfide bridging or chelating ligand synthons for the synthesis of new types of polynuclear complexes and coordination polymers as well.",
keywords = "clathrochelate, cluster, iron complexes, ligand reactivity, nucleophilic substitution, SUBSTITUENTS, CLATHROCHELATE, HYBRID",
author = "Ogienko, {M. A.} and Konchenko, {S. N.} and Burdukov, {A. B.} and Vologzhanina, {A. V.} and Lebed, {E. G.} and Voloshin, {Y. Z.}",
year = "2018",
month = aug,
day = "1",
doi = "10.1134/S1070328418080055",
language = "English",
volume = "44",
pages = "496--501",
journal = "Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya",
issn = "1070-3284",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "8",

}

RIS

TY - JOUR

T1 - Unexpected Product of the Reaction of Iron(II) Dichloroclathrochelate with the [Fe2(μ-S)2(CO)6]2– Cluster Dianion

T2 - Synthesis and X-ray Diffraction Structure of the First Cage Complex with Thiol Groups Inherently Bonded to a Macrobicyclic Framework

AU - Ogienko, M. A.

AU - Konchenko, S. N.

AU - Burdukov, A. B.

AU - Vologzhanina, A. V.

AU - Lebed, E. G.

AU - Voloshin, Y. Z.

PY - 2018/8/1

Y1 - 2018/8/1

N2 - An attempt to prepare a hybrid clusteroclathrochelate by nucleophilic substitution of iron(II) dichloroclathrochelate by substitution of its chlorine atoms with the [Fe2(μ-S)2(CO)6]2– cluster dianion as a nucleophilic agent generated in situ by the reduction of Fe2(μ-S2)(CO)6 with lithium triethylborohydride unexpectedly gave the macrobicyclic complex with two inherent thiol groups as the single clathrochelate product. Obviously, the initial iron-sulfide cluster underwent a complete decomposition during the reaction, thus acting only as a source of HS– and S2– anions. The composition and the structure of the complex obtained were confirmed by elemental analysis, MALDI-TOF mass spectrometry, 1H and 13C{1H} NMR spectroscopy, and single crystal X-ray diffraction (CIF file CCDC 1585112). The encapsulated iron(II) ion is located at the centre of its FeN6 coordination polyhedron possessing the geometry intermediate between a trigonal prism (the distortion angle φ = 0°) and a trigonal antiprism (φ = 60°) with φ ≈ 25°; the height of this polyhedron is 2.33 Å. The presence of two thiol groups in the vicinal positions of the same ribbed moiety of the macrobicyclic molecule substantially affects the crystal packing of the molecular crystal containing clathrochelate dimers formed by four hydrogen bonds of two types (i.e., two S–H···O and two S–H···N bonds). The obtained cage complex and its deprotonated forms seem to be promising cis-disulfide bridging or chelating ligand synthons for the synthesis of new types of polynuclear complexes and coordination polymers as well.

AB - An attempt to prepare a hybrid clusteroclathrochelate by nucleophilic substitution of iron(II) dichloroclathrochelate by substitution of its chlorine atoms with the [Fe2(μ-S)2(CO)6]2– cluster dianion as a nucleophilic agent generated in situ by the reduction of Fe2(μ-S2)(CO)6 with lithium triethylborohydride unexpectedly gave the macrobicyclic complex with two inherent thiol groups as the single clathrochelate product. Obviously, the initial iron-sulfide cluster underwent a complete decomposition during the reaction, thus acting only as a source of HS– and S2– anions. The composition and the structure of the complex obtained were confirmed by elemental analysis, MALDI-TOF mass spectrometry, 1H and 13C{1H} NMR spectroscopy, and single crystal X-ray diffraction (CIF file CCDC 1585112). The encapsulated iron(II) ion is located at the centre of its FeN6 coordination polyhedron possessing the geometry intermediate between a trigonal prism (the distortion angle φ = 0°) and a trigonal antiprism (φ = 60°) with φ ≈ 25°; the height of this polyhedron is 2.33 Å. The presence of two thiol groups in the vicinal positions of the same ribbed moiety of the macrobicyclic molecule substantially affects the crystal packing of the molecular crystal containing clathrochelate dimers formed by four hydrogen bonds of two types (i.e., two S–H···O and two S–H···N bonds). The obtained cage complex and its deprotonated forms seem to be promising cis-disulfide bridging or chelating ligand synthons for the synthesis of new types of polynuclear complexes and coordination polymers as well.

KW - clathrochelate

KW - cluster

KW - iron complexes

KW - ligand reactivity

KW - nucleophilic substitution

KW - SUBSTITUENTS

KW - CLATHROCHELATE

KW - HYBRID

UR - http://www.scopus.com/inward/record.url?scp=85052586353&partnerID=8YFLogxK

U2 - 10.1134/S1070328418080055

DO - 10.1134/S1070328418080055

M3 - Article

AN - SCOPUS:85052586353

VL - 44

SP - 496

EP - 501

JO - Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya

JF - Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya

SN - 1070-3284

IS - 8

ER -

ID: 25413447