Erratum: Negishi cross-coupling reaction catalyzed by an aliphatic, phosphine based pincer complex of palladium. biaryl formation via cationic pincer-type PdIV intermediates (Dalton Transactions (2011) 40 (8996) DOI: 10.1039/C1DT10398A)

Full text of DOI:10.1039/C1DT90189C

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ADDITIONS & CORRECTIONS
Square structures and photophysical properties of Zn2Ln2 complexes (Ln = Nd, Eu, Sm, Er, Yb)
Hai-Bing Xu, Hui-Min Wen, Zhong-Hui Chen, Jia Li, Lin-Xi Shi and Zhong-Ning Chen
Dalton Trans., 2010, 39, 1948 (DOI: 10.1039/b919170D). Amendment published 14thJanuary 2011.
In the published version of this paper the chromaticity coordinates for complex 4 reported on page 1951 are incorrect and should be
changed to CIE = (0.35, 0.34). The corrected chromaticity diagram of 4 (Fig. 7) is shown below.
Fig. 7 The chromaticity coordinates of 4 after irradiation with 345 nm in dichloromethane at 298 K.
Multimodal radio- (PET/SPECT) and fluorescence imaging agents based on metallo-radioisotopes: current applications and prospects for
development of new agents
Flora L. Thorp-Greenwood and Michael P. Coogan
Dalton Trans., 2011, 40 (DOI: 10.1039/C0DT01398F). Amendment published 20thJanuary 2011.
In the published version of this paper there was a typographical error in reference number 64; the article was published in the Journal of
Biological Inorganic Chemistry (J. Biol. Inorg. Chem.) not the Journal of Biological Chemistry.
The correct reference 64 is shown below:
S. Lim, K. A. Price, S. Chong, B. M. Paterson, A. Caragounis, K. J. Barnham, P. J. Crouch, J. M. Peach, J. R. Dilworth, A. R. White
and Paul S. Donnelly, J. Biol. Inorg. Chem., 2010, 15, 225.
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Syntheses, structures and photophysical properties of heterotrinuclear Zn2Ln clusters (Ln = Nd, Eu, Tb, Er, Yb)
Hai-Bing Xu, Ye-Teng Zhong, Wei-Xiong Zhang, Zhong-Ning Chen and Xiao-Ming Chen
Dalton Trans., 2010, 39, 5676 (DOI: 10.1039/C000783H). Amendment published 14thJanuary 2011.
In the published version of this paper the chromaticity coordinates for complex 3 reported on page 5679 are incorrect and should be
changed to CIE = (0.43, 0.35). The corrected chromaticity diagram of 3 (Fig. S4 of the supplementary information) is shown below.
Fig. S4 The chromaticity coordinates of 3 after irradiation with 338 nm in dichloromethane at 298 K.
Chemistry and applications of organotin(IV) complexes of Schiff bases
Mala Nath and Pramendra K. Saini
Dalton Trans., 2011, 40 (DOI: 10.1039/C0DT01426E). Amendment published 17thMay 2011.
In the published version of this paper there was a typographical error in Pramendra K. Saini’s biography; the year in which he obtained
his PhD was 2009, not 2008.
The correct sentence from the biography is shown below:
Pramendra Kumar Saini did his MSc at CCS University, Meerut, and thereafter he joined as a Project Fellow in 2002 under a UGC
sponsored research project, and then joined as a CSIR-JRF in 2003 and completed his PhD in 2009 under the supervision of Prof. Mala
Nath at the Indian Institute of Technology Roorkee.
12936 | Dalton Trans., 2011, 40, 12935–12942
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Novel layered crystalline zinc poly(styrene-phenylvinyl phosphonate)-phosphate synthesized by a simple route in a THF–water medium
Jing Huang, Xiangkai Fu, Gang Wang, Chao Li and Xiaoyan Hu
Dalton Trans., 2011, 40, 3631–3639 (DOI: 10.1039/C0DT01553A). Amendment published 27thJuly 2011.
The address for the authors should be:
College of Chemistry and Chemical Engineering Southwest University, Research Institute of Applied Chemistry Southwest University,
The Key Laboratory of Applied Chemistry of Chongqing Municipality, The Key Laboratory of Eco-environments in Three Gorges
Reservoir Region Ministry of Education, Chongqing, 400715, P. R. China; Tel: +86 23 68253704; Fax: +86 23 68254000. E-mail:
fxk@swu.edu.cn
Synthesis, characterization and catalytic activity of magnesium and zinc aminophenoxide complexes: Catalysts for ring-opening
polymerization of L-lactide
Hui-Ju Chuang, Shi-Feng Weng, Chia-Chih Chang, Chu-Chieh Lin and Hsuan-Ying Chen
Dalton Trans., 2011, 40, 9601–9607 (DOI: 10.1039/10.1039/C1DT11080B). Amendment published 4thOctober 2011.
In Ref. 7 the following two references were inadvertently omitted by the authors:
Ref. 7 (k) V. Poirier, T. Roisnel, J.-F. Carpentier and Y. Sarazin, Dalton Trans., 2009, 40, 9820; (l) V. Poirier, T. Roisnel, J.-F. Carpentier
and Y. Sarazin, Dalton Trans., 2011, 40, 523.
Structures, electronic properties and solid state luminescence of Cu(I) iodide complexes with 2,9-dimethyl-1,10-phenanthroline and aliphatic
aminomethylphosphines or triphenylphosphine
Radosław Starosta, Małgorzata Puchalska, Joanna Cybin´ska, Maciej Barys and Anja V. Mudring
Dalton Trans., 2011, 40 (DOI: 10.1039/C0DT01284J). Amendment published 2nd February 2011.
In the published version of this paper there was an error in Table 3. The correct values are shown below:
1P
3P
4P
1N
3N
4N
1A1
d(CuI)
2.6616
2.6504
2.6337
2.6861
2.6775
2.6490
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Holo-Ni2+ Helicobacter pylori NikR contains four square-planar nickel-binding sites at physiological pH
Stefano Benini, Michele Cianci and Stefano Ciurli
Dalton Trans., 2011, 40, 7831 (DOI: 10.1039/C1DT11107H). Amendment published 28thSeptember 2011.
On page 7832 of the above article the author would like to change the following sentence from
“To avoid the possible influence of crystal packing strain on the Ni2+ binding event, HpNikR was later crystallized from a solution
containing Ni2+, at pH 5.6.14”
to
“To avoid the possible influence of crystal packing strain on the Ni2+ binding event, HpNikR isolated in the holo-form was later
crystallized at pH 5.6.14”
Supramolecular networks of polymethylphosphonic acid groups bonded to aromatic platforms: biphenyldiyl-2,2¢-bis(methylphosphonic acid)
and benzenetriyl-1,3,5-tris(methylphosphonic acid)
Jerzy Zon´, Deyuan Kong, Kevin Gagnon, Houston Perry, LeAnthony Holliness and Abraham Clearfield
Dalton Trans., 2010, 39, 11008 (DOI: 10.1039/c0dt00676a). Amendment published 19thNovember 2010.
In the published version of Scheme 1, there should have been an additional PO3H2 group attached to the right-hand side of structure IV
and structure VII and the structure labelled as BBMP should have been labelled as VI BBMP.
The correct Scheme 1 is shown below:
Scheme 1 Conformationally rigid (II, V) and flexible phosphonic acids.
12938 | Dalton Trans., 2011, 40, 12935–12942
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Monosubstituted arylimido hexamolybdates containing pendant amino groups: synthesis and structural characterization
Yi Zhu, Zicheng Xiao, Longsheng Wang, Panchao Yin, Jian Hao, Yongge Wei and Yuan Wang
Dalton Trans., 2011, 40, 7304–7309 (DOI: 10.1039/C1DT10168D). Amendment published 18thJuly 2011.
On page 1, the word ‘not’ should be removed from the sentence ‘However, compared with the intensive investigations on such Anderson-
type derivatives, organically modified Lindqvist-type POMs with pendant amino groups have rarely been reported to date (except only
one example of bifunctionalized phenylenediamine derivative of hexamolybdates which was not determined by single-crystal X-ray
diffraction12).¢
In fact, in his paper (ref. 12) Professor R. John Errington has described the synthesis as well as the crystal structure of the first
bifunctionalized phenylenediamine derivative of hexamolybdates.
Negishi cross-coupling reaction catalyzed by an aliphatic, phosphine based pincer complex of palladium. biaryl formation via cationic
pincer-type PdIV intermediates
Roman Gerber, Olivier Blacque and Christian M. Frech
Dalton Trans., 2011, 40, 8996 (DOI: 10.1039/C1DT10398A). Amendment published 26thOctober 2011.
The authors apologise that in the above article all of the conversions and yields for the Negishi cross-coupling reactions are the same in
Tables 1–4. The corrected tables with correct conversions and yields are displayed below.
Table 1 Negishi cross-coupling reactions of aryl bromides with diphenylzinc catalyzed by 1a
a Reaction conditions: 2.0 mmol aryl halide, 1.4 mmol diphenylzinc, 4 ml NMP, catalyst (0.01 mol%) added in solution (dioxane), reaction performed at
100 ◦C. Conversions determined by GC/MS, based on aryl halide. b2.8 mmol of diphenylzinc was used.
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Table 2 Negishi cross-coupling reactions of aryl bromides with bis(4-methoxyphenyl)zinc and bis[4-(dimethylamino)phenyl]zinc catalyzed by 1a
a Reaction conditions: 2.0 mmol aryl halide, 1.4 mmol diphenylzinc, 4 ml NMP, catalyst (0.01 mol%) added in solution (dioxane), reaction performed at
100 ◦C. Conversions determined by GC/MS, based on aryl halide. b2.8 mmol of the diarylzinc was used.
Table 3 Negishi cross-coupling reactions of aryl bromides with bis(2-methylphenyl)zinc and bis(2,4,6-trimethylphenyl)zinc catalyzed by 1a
a Reaction conditions: 2.0 mmol aryl halide, 1.4 mmol diphenylzinc, 4 ml NMP, catalyst (0.01 mol%) added in solution (dioxane), reaction performed at
100 ◦C. Conversions determined by GC/MS, based on aryl halide. b2.8 mmol of the diarylzinc was used.
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Table 4 Negishi cross-coupling reactions of aryl bromides with dithiophen-3-ylzinc catalyzed by 1a
a Reaction conditions: 2.0 mmol aryl halide, 1.4 mmol dithiophen-3-ylzinc, 4 ml NMP, catalyst (0.01 mol%) added in solution (dioxane), reaction
performed at 100 ◦C. Conversions determined by GC/MS, based on aryl halide.
Crystalline metal (Li, Mg, Ca, Sr, Ba, Sn, Pb) complexes of the new chelating N,N¢-dianionic [1,2-N(R)C6H4(CH2NR)]2- ligand (R =
SiMe3, CH2But)
Catherine F. Caro, Martyn P. Coles, Peter B. Hitchcock, Michael F. Lappert and Luc J.-M. Pierssens
Dalton Trans., 2011, 40, 9821 (DOI: 10.1039/C1DT10574D). Amendment published 6thOctober 2011.
The authors overlooked the following paper which described three of our compounds (2, 4a, 4b), including the X-ray structures of two
of them:
R. M. Gauvin, N. Kyritsakas, J. Fischer and J. Kress, Chem. Commun., 2000, 965.
Data for the three compounds were first revealed in the D. Phil (Sussex) thesis of C. F. Caro.
Relaxation dynamics of dysprosium(III) single molecule magnets
Yun-Nan Guo, Gong-Feng Xu, Yang Guo and Jinkui Tang
Dalton Trans., 2011, 40, 9953 (DOI: 10.1039/C1DT10474H). Amendment published 3rd October 2011.
The sum of two modified Debye functions in Eqn. (5) and (6) contain a typographical error; it should read:
In our work, of course, we used these correct equations. Thus, none of our results are affected in any way by the misprint.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
Additions and corrections can be viewed online by accessing the original article to which they apply.
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