Nitridomanganese(V) and -(VI) complexes containing macrocyclic amine ligands

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Standard

Nitridomanganese(V) and -(VI) complexes containing macrocyclic amine ligands. / Meyer, Karsten; Bendix, Jesper; Metzler-Nolte, Nils; Weyhermüller, Thomas; Wieghardt, Karl.

I: Journal of the American Chemical Society, Bind 120, Nr. 29, 29.07.1998, s. 7260-7270.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Meyer, K, Bendix, J, Metzler-Nolte, N, Weyhermüller, T & Wieghardt, K 1998, 'Nitridomanganese(V) and -(VI) complexes containing macrocyclic amine ligands', Journal of the American Chemical Society, bind 120, nr. 29, s. 7260-7270. https://doi.org/10.1021/ja980686j

APA

Meyer, K., Bendix, J., Metzler-Nolte, N., Weyhermüller, T., & Wieghardt, K. (1998). Nitridomanganese(V) and -(VI) complexes containing macrocyclic amine ligands. Journal of the American Chemical Society, 120(29), 7260-7270. https://doi.org/10.1021/ja980686j

Vancouver

Meyer K, Bendix J, Metzler-Nolte N, Weyhermüller T, Wieghardt K. Nitridomanganese(V) and -(VI) complexes containing macrocyclic amine ligands. Journal of the American Chemical Society. 1998 jul 29;120(29):7260-7270. https://doi.org/10.1021/ja980686j

Author

Meyer, Karsten ; Bendix, Jesper ; Metzler-Nolte, Nils ; Weyhermüller, Thomas ; Wieghardt, Karl. / Nitridomanganese(V) and -(VI) complexes containing macrocyclic amine ligands. I: Journal of the American Chemical Society. 1998 ; Bind 120, Nr. 29. s. 7260-7270.

Bibtex

@article{365766501c314af687f6723dad8a413e,
title = "Nitridomanganese(V) and -(VI) complexes containing macrocyclic amine ligands",
abstract = "Photolysis of trans-[(cyclam)Mn(III)(N3)2](ClO4) (1) in methanol at - 35 °C with ~350 nm light produces blue [{trans-[(cyclam)Mn(V)(N)]}2(μ- N3)](ClO4)3·3H2O (2) and dinitrogen (cyclam = 1,4,8,11- tetraacyclotetradecane). A series of six-coordinate complexes trans- [(cyclam)Mn(V)(N)Y](n+), where Y represents Cl, n = 1 (3); CH3CN, n = 2 (4); ClO4-, n = 1 (5); CF3CO2-, n = 1 (6), was also synthesized. From a methanol solution of 2 and addition of NaCN the species cis- [(cyclam)Mn(V)(N)(CN)](ClO4) (7) was obtained. Photolysis of [LMn(III)(N3)3], where L represents the macrocycle 1,4,7-trimethyl-1,4,7- triazacyclononane, in CH3CN at 20 °C with 253.7 nm light produces colorless crystals of [{LMn(II)(N3)}2(μ-N3)2] (8) (photoreduction), whereas photolysis with 350 nm light at -35 °C gives the blue photooxidation product [LMn(V)(N)(N3)2] (9). Complexes 1-7 were characterized by X-ray crystallography. Compounds 2-7 contain the nitridomanganese(V) unit (Mn≡ N 1.51-1.54 {\AA}). All nitridomanganese(V) complexes display significant temperature-independent paramagnetism indicative of a low-spin d2 electron configuration. In the electronic spectra four d-d transitions have been identified for the first time which were unambiguously assigned by single crystal polarized UV/vis/NIR and magnetic circular dichroism (MCD) spectroscopy. The spectra were satisfactorily analyzed in the frame of ligand-field theory (angular overlap method). 15N NMR spectroscopy revealed an enormous deshielding of the nitrido group in 4, 6, and 7 (δ = 693-699 ppm referenced to CH3NO2 at 0 ppm). Electrochemically, complex 4 undergoes a reversible one-electron oxidation generating a stable nitridomanganese(VI) species (d1) which has been characterized by UV-Vis and EPR spectroscopy.",
author = "Karsten Meyer and Jesper Bendix and Nils Metzler-Nolte and Thomas Weyherm{\"u}ller and Karl Wieghardt",
year = "1998",
month = jul,
day = "29",
doi = "10.1021/ja980686j",
language = "English",
volume = "120",
pages = "7260--7270",
journal = "Journal of the American Chemical Society",
issn = "0002-7863",
publisher = "ACS Publications",
number = "29",

}

RIS

TY - JOUR

T1 - Nitridomanganese(V) and -(VI) complexes containing macrocyclic amine ligands

AU - Meyer, Karsten

AU - Bendix, Jesper

AU - Metzler-Nolte, Nils

AU - Weyhermüller, Thomas

AU - Wieghardt, Karl

PY - 1998/7/29

Y1 - 1998/7/29

N2 - Photolysis of trans-[(cyclam)Mn(III)(N3)2](ClO4) (1) in methanol at - 35 °C with ~350 nm light produces blue [{trans-[(cyclam)Mn(V)(N)]}2(μ- N3)](ClO4)3·3H2O (2) and dinitrogen (cyclam = 1,4,8,11- tetraacyclotetradecane). A series of six-coordinate complexes trans- [(cyclam)Mn(V)(N)Y](n+), where Y represents Cl, n = 1 (3); CH3CN, n = 2 (4); ClO4-, n = 1 (5); CF3CO2-, n = 1 (6), was also synthesized. From a methanol solution of 2 and addition of NaCN the species cis- [(cyclam)Mn(V)(N)(CN)](ClO4) (7) was obtained. Photolysis of [LMn(III)(N3)3], where L represents the macrocycle 1,4,7-trimethyl-1,4,7- triazacyclononane, in CH3CN at 20 °C with 253.7 nm light produces colorless crystals of [{LMn(II)(N3)}2(μ-N3)2] (8) (photoreduction), whereas photolysis with 350 nm light at -35 °C gives the blue photooxidation product [LMn(V)(N)(N3)2] (9). Complexes 1-7 were characterized by X-ray crystallography. Compounds 2-7 contain the nitridomanganese(V) unit (Mn≡ N 1.51-1.54 Å). All nitridomanganese(V) complexes display significant temperature-independent paramagnetism indicative of a low-spin d2 electron configuration. In the electronic spectra four d-d transitions have been identified for the first time which were unambiguously assigned by single crystal polarized UV/vis/NIR and magnetic circular dichroism (MCD) spectroscopy. The spectra were satisfactorily analyzed in the frame of ligand-field theory (angular overlap method). 15N NMR spectroscopy revealed an enormous deshielding of the nitrido group in 4, 6, and 7 (δ = 693-699 ppm referenced to CH3NO2 at 0 ppm). Electrochemically, complex 4 undergoes a reversible one-electron oxidation generating a stable nitridomanganese(VI) species (d1) which has been characterized by UV-Vis and EPR spectroscopy.

AB - Photolysis of trans-[(cyclam)Mn(III)(N3)2](ClO4) (1) in methanol at - 35 °C with ~350 nm light produces blue [{trans-[(cyclam)Mn(V)(N)]}2(μ- N3)](ClO4)3·3H2O (2) and dinitrogen (cyclam = 1,4,8,11- tetraacyclotetradecane). A series of six-coordinate complexes trans- [(cyclam)Mn(V)(N)Y](n+), where Y represents Cl, n = 1 (3); CH3CN, n = 2 (4); ClO4-, n = 1 (5); CF3CO2-, n = 1 (6), was also synthesized. From a methanol solution of 2 and addition of NaCN the species cis- [(cyclam)Mn(V)(N)(CN)](ClO4) (7) was obtained. Photolysis of [LMn(III)(N3)3], where L represents the macrocycle 1,4,7-trimethyl-1,4,7- triazacyclononane, in CH3CN at 20 °C with 253.7 nm light produces colorless crystals of [{LMn(II)(N3)}2(μ-N3)2] (8) (photoreduction), whereas photolysis with 350 nm light at -35 °C gives the blue photooxidation product [LMn(V)(N)(N3)2] (9). Complexes 1-7 were characterized by X-ray crystallography. Compounds 2-7 contain the nitridomanganese(V) unit (Mn≡ N 1.51-1.54 Å). All nitridomanganese(V) complexes display significant temperature-independent paramagnetism indicative of a low-spin d2 electron configuration. In the electronic spectra four d-d transitions have been identified for the first time which were unambiguously assigned by single crystal polarized UV/vis/NIR and magnetic circular dichroism (MCD) spectroscopy. The spectra were satisfactorily analyzed in the frame of ligand-field theory (angular overlap method). 15N NMR spectroscopy revealed an enormous deshielding of the nitrido group in 4, 6, and 7 (δ = 693-699 ppm referenced to CH3NO2 at 0 ppm). Electrochemically, complex 4 undergoes a reversible one-electron oxidation generating a stable nitridomanganese(VI) species (d1) which has been characterized by UV-Vis and EPR spectroscopy.

UR - http://www.scopus.com/inward/record.url?scp=0032578159&partnerID=8YFLogxK

U2 - 10.1021/ja980686j

DO - 10.1021/ja980686j

M3 - Journal article

AN - SCOPUS:0032578159

VL - 120

SP - 7260

EP - 7270

JO - Journal of the American Chemical Society

JF - Journal of the American Chemical Society

SN - 0002-7863

IS - 29

ER -

ID: 240004312