Publikationen
Trefoil-Shaped Porous Nanographenes Bearing a Tribenzotriquinacene Core by Three-fold Scholl Macrocyclization
L. He, C.-F. Ng, Y. Li, Z. Liu, D. Kuck, H.-F. Chow, Angew. Chem. Int. Ed. 57 (2018) 13635–13639.
DOI: 10.1002/anie.201808461
DOI: 10.1002/anie.201808461
Stereoselective synthesis of enantiomerically pure bowl-shaped hydroxytribenzotriquinacenes
P. Rommelmann, B. Nachtigall, T. Guntelmann, H. Gröger, D. Kuck, Org. Biomol. Chem. 16 (2018) 5636–5642.
DOI: 10.1039/C8OB01425F
DOI: 10.1039/C8OB01425F
Back Cover:
Dodecabromo- and Dodecaiodocentrohexaindane: Td-Symmetrical Key Building Blocks for Twelvefold Cross Coupling Reactions and Sixfold Orthogonal Extension
Dodecabromo- and Dodecaiodocentrohexaindane: Td-Symmetrical Key Building Blocks for Twelvefold Cross Coupling Reactions and Sixfold Orthogonal Extension
J. Linke, B. Neumann, H.-G. Stammler, D. Kuck, Eur. J. Chem. 24 (2018) 9316–9324.
DOI: 10.1002/chem.201801806
DOI: 10.1002/chem.201801806
Cover:
Combining Stereoselective Enzyme Catalysis with Chirality-Assisted Synthesis in Tribenzotriquinacene Chemistry
Combining Stereoselective Enzyme Catalysis with Chirality-Assisted Synthesis in Tribenzotriquinacene Chemistry
P. Rommelmann, W. Greschner, S. Ihrig, B. Neumann, H.-G. Stammler, H. Gröger, D. Kuck, Eur. J. Org. Chem. (2018) 3891–3899.
DOI: 10.1002/ejoc.201800465
DOI: 10.1002/ejoc.201800465
Feature Article:
Biconcave and Convex-Concave Tribenzotriquinacene Dimers
Biconcave and Convex-Concave Tribenzotriquinacene Dimers
Z.-M. Li, Y.-W. Li, X.-P. Cao, H.-F. Chow, D. Kuck, J. Org. Chem. 83 (2018) 3343–3440.
DOI: 10.1021/acs.joc.8b00375
DOI: 10.1021/acs.joc.8b00375
Sixfold Peripheral Halogenation of Tribenzotriquinacenes: An Alternative Access to Useful TBTQ Building Blocks
J. Linke, N. Bader, J. Tellenbröker, D. Kuck, Synthesis 50 (2018) 175–183.
DOI: 10.1055/s-0036-1589107
DOI: 10.1055/s-0036-1589107
An Efficient Ag+-Selective Fluorescent Chemosensor Derived from Tribenzotriquinacene
Z.-M. Li, D. Hu, J. Wei ,Q. Qi, X.-P. Cao, H.-F. Chow, D. Kuck, Synthesis 50 (2018) 1457–1461.
DOI: 10.1055/s-0036-1591759
DOI: 10.1055/s-0036-1591759
Synthesis and characterization of a novel difluoromethylene phosphonic acid functionalized polymer
C. Alter, B. Hoge, J. Appl. Polym. Sci. (2018) in print.
DOI: 10.1002/app.46765
DOI: 10.1002/app.46765
Coordination Chemistry of the Tris(pentafluoroethyl)stannate(II) Anion, [Sn(C2F5)3]−
J. Klösener, M. Wiesemann, B. Neumann, H.-G. Stammler, B. Hoge, Eur. J. Inorg. Chem. (2018) 3971–3977.
DOI: 10.1002/ejic.201800796
DOI: 10.1002/ejic.201800796
Hypercoordinated Fluoro(pentafluoroethyl)stannanes and -stannates
J. Klösener, M. Wiesemann, B. Neumann, H.-G. Stammler, B. Hoge, Eur. J. Inorg. Chem. (2018) 3960–3970.
DOI: 10.1002/ejic.201800795
DOI: 10.1002/ejic.201800795
Reviews Showcase:
Pentafluoroethylated Compounds of Silicon, Germanium and Tin
Pentafluoroethylated Compounds of Silicon, Germanium and Tin
M. Wiesemann, B. Hoge, Chem. Eur. J. 24 (2018) im Druck.
DOI: 10.1002/chem.201801292
DOI: 10.1002/chem.201801292
Hot Paper + Cover Feature:
Activation of CH3CN with (C2F5)3PF2 and amines
Activation of CH3CN with (C2F5)3PF2 and amines
J. Bader, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 24 (2018) 6975–6982.
DOI: 10.1002/chem.201800682
DOI: 10.1002/chem.201800682
Hot Paper:
Synthesis and Reactivity of Donor-Stabilized Bis(pentafluoroethyl)stannylene [Sn(C2F5)2(D)n] (D=THF, DMAP, PMe3, [Sn(C2F5)3]−)
Synthesis and Reactivity of Donor-Stabilized Bis(pentafluoroethyl)stannylene [Sn(C2F5)2(D)n] (D=THF, DMAP, PMe3, [Sn(C2F5)3]−)
J. Klösener, M. Wiesemann, M. Niemann, B. Neumann, H.-G. Stammler, B. Hoge, Chem. Eur. J. 24 (2018) 4412–4422.
DOI: 10.1002/chem.201705770
DOI: 10.1002/chem.201705770
The Dynamic Equilibrium of Hexakis(pentafluoroethyl)distannane Adducts [XSn(C2F5)3{Sn(C2F5)3}]−
(X=Cl, Br, I, Sn(C2F5)3)
M. Wiesemann, J. Klösener, B. Neumann, H.-G. Stammler, B. Hoge, Chem. Eur. J. 24 (2018) 4336–4342.
DOI: 10.1002/chem.201705069
DOI: 10.1002/chem.201705069
VIP:
Syntheses of stable salts containing the hydridophosphate anion [P(C2F5)3F2H]−
Syntheses of stable salts containing the hydridophosphate anion [P(C2F5)3F2H]−
J. Bader, N. Ignat'ev, B. Hoge, Eur. J. Inorg. Chem. 2018 (2018) 861–866.
DOI: 10.1002/ejic.201701375
DOI: 10.1002/ejic.201701375
Bis(diethylamino)pentafluorophenylphosphane as Valuable Precursor for the Design of Tetrafluorophenylphosphanes, Tetrafluorophenylphosphinic and -phosphonic Acids
C. Alter, B. Neumann, H.-G. Stammler, B. Hoge, Eur. J. Inorg. Chem. 2018 (2018) 867–875.
DOI: 10.1002/ejic.201701402
DOI: 10.1002/ejic.201701402
Tris(pentafluoroethyl)stannane: Tin Hydride Chemistry with an Electron-Deficient Stannane
M. Wiesemann, M. Niemann, J. Klösener, B. Neumann, H.-G. Stammler, B. Hoge, Chem. Eur. J. 24 (2018) 2699–2708.
DOI: 10.1002/chem.201705068
DOI: 10.1002/chem.201705068
Metal-free dehydrogenation of tri- and diethylamine with (C2F5)3PF2
J. Bader, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, J. Fluorine Chem. 207 (2018) 12–17.
DOI: 10.1016/j.jfluchem.2017.12.015
DOI: 10.1016/j.jfluchem.2017.12.015
Hot Paper + Cover Feature:
On Pentakis(pentafluoroethyl)stannate, [Sn(C2F5)5]−, and the Gas-Free Generation of Pentafluoroethyllithium, LiC2F5
On Pentakis(pentafluoroethyl)stannate, [Sn(C2F5)5]−, and the Gas-Free Generation of Pentafluoroethyllithium, LiC2F5
M. Wiesemann, J. Klösener, B. Neumann, H.-G. Stammler, B. Hoge, Chem. Eur. J. 24 (2018) 1838–1843.
DOI: 10.1002/chem.201704807
DOI: 10.1002/chem.201704807
From Fenestrindane Toward Saddle-Shaped Nanographenes Bearing a Tetracoordinate Carbon Atom
W.-S. Wong, C.-F. Ng, D. Kuck, H.-F. Chow, Angew. Chem. 129 (2017) 12528–12532; Angew. Chem. Int. Ed. 56 (2017) 12356–12360.
DOI: 10.1002/ange.201707505; DOI: 10.1002/anie.201707505 (Int. Ed.)
DOI: 10.1002/ange.201707505; DOI: 10.1002/anie.201707505 (Int. Ed.)
An Elusive Nonaromatic Goal behind the Centropolyindanes: Aufbau of Veratrolo-annelated Centropolyquinanes and Ozonolytic Abbau
M. Harig, B. Neumann, H.-G. Stammler, D. Kuck, ChemPlusChem 82 (2017) 1087–1095.
DOI: 10.1002/cplu.201700090
DOI: 10.1002/cplu.201700090
Host-Guest Complexes of a Tribenzotriquinacene-Based Tris(catechol) with Quaternary Ammonium Salts: Variation of H-Bonding Pattern and Cationic Size on Supramolecular Architecture
C.-F. Ng, H.-F. Chow, D. Kuck, T. C. W. Mak, Cryst. Growth Des. 17 (2017) 2822–2827.
DOI: 10.1021/acs.cgd.7b00278
DOI: 10.1021/acs.cgd.7b00278
Electronic and Steric Effects on the Three-fold Scholl-Type Cycloheptatriene Ring Formation Around a Tribenzotriquinacene Core
H.-W. Ip, H.-F. Chow, D. Kuck, Org. Chem. Front. 4 (2017) 817–822.
DOI: 10.1039/C7QO00132K
DOI: 10.1039/C7QO00132K
Tribenzotriquinacene-Based Crown Ethers – Synthesis and Selective Complexation with Ammonium Salts
Y.-F. Zhang, X.-P. Cao, H.-F. Chow, D. Kuck, J. Org. Chem. 82 (2017) 179–187.
DOI: 10.1021/acs.joc.6b02326
DOI: 10.1021/acs.joc.6b02326
A Cyclopenta[hi]acephenanthrylene Bearing Two Benzoannelated [3.3.3]Propellane Units: Extension of Triptindane Chemistry
T. Hackfort, B. Neumann, H.-G. Stammler, D. Kuck, Can. J. Chem. 95 (2017) 390–398.
DOI: 10.1139/cjc-2016-0498
DOI: 10.1139/cjc-2016-0498
Hot Paper + Cover Feature:
The Tris(pentafluoroethyl)stannate(II) Anion, [Sn(C2F5)3]− – Synthesis and Reactivity
The Tris(pentafluoroethyl)stannate(II) Anion, [Sn(C2F5)3]− – Synthesis and Reactivity
M. Wiesemann, J. Klösener, M. Niemann, B. Neumann, H.-G. Stammler, B. Hoge, Chem. Eur. J. 23 (2017) 14476–14484.
DOI: 10.1002/chem.201702855
DOI: 10.1002/chem.201702855
VIP + Front Cover + Cover Profile:
Solid-State Structure of a Bromo(difluoromethylenephosphonato)cuprate - a Key Intermediate for the Synthesis of α,α-Difluoromethylenephosphonates
Solid-State Structure of a Bromo(difluoromethylenephosphonato)cuprate - a Key Intermediate for the Synthesis of α,α-Difluoromethylenephosphonates
C. Alter, B. Neumann, H.-G. Stammler, L. Weber, B. Hoge, Eur. J. Inorg. Chem. 2017 (2017) 3489–3493.
DOI: 10.1002/ejic.201700526
DOI: 10.1002/ejic.201700526
Perfluoroalkylated Main-Group Element Lewis Acids as Catalysts in Transfer Hydrogenation
J. Bader, A. F. G. Maier, J. Paradies, B. Hoge, Eur. J. Inorg. Chem. 2017 (2017) 3053–3056.
DOI: 10.1002/ejic.201700524
DOI: 10.1002/ejic.201700524
Synthesis of Mono-, Bis- and Tris(pentafluoroethyl)tin Derivatives, (C2F5)4–nSnXn (X=Ph, Me, Cl, Br, Cp; n = 1–3)
J. Klösener, M. Wiesemann, M. Niemann, B. Neumann, H.-G. Stammler, B. Hoge, Chem. Eur. J. 23 (2017) 8295–8303.
DOI: 10.1002/chem.201701270
DOI: 10.1002/chem.201701270
Feature:
Synthesis and Characterization of Tetrakis(pentafluoroethyl)germane
Synthesis and Characterization of Tetrakis(pentafluoroethyl)germane
S. Pelzer, B. Neumann, H.-G. Stammler, N. Ignat'ev, R. Eujen, B. Hoge, Synthesis 49 (2017) 2389–2393.
DOI: 10.1055/s-0036-1589005
DOI: 10.1055/s-0036-1589005
Hot Paper:
Tris(pentafluoroethyl)germane: Deprotonation and Hydrogermylation Reactions
Tris(pentafluoroethyl)germane: Deprotonation and Hydrogermylation Reactions
S. Pelzer, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 23 (2017) 12233–12242.
DOI: 10.1002/chem.201700634
DOI: 10.1002/chem.201700634
Hot Paper + Back Cover:
Pentafluoroethyl Bismuth Compounds
Pentafluoroethyl Bismuth Compounds
S. Solyntjes, J. Bader, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 23 (2017) 1557–1567.
DOI: 10.1002/chem.201604910
DOI: 10.1002/chem.201604910
Bismuth Perfluoroalkylphosphinates: New Catalysts for Application in Organic Syntheses
S. Solyntjes, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 23 (2017) 1568–1575.
DOI: 10.1002/chem.201604914
DOI: 10.1002/chem.201604914
Boreal pollen contain ice-nucleating as well as ice-binding antifreeze polysaccharides
K. Dreischmeier, C. Budke, L. Wiehemeier, T. Kottke, T. Koop, Sci. Rep. 7 (2017) 41890.
DOI: 10.1038/srep41890
DOI: 10.1038/srep41890
1,3,2-Diazaboryl Anions - From Laboratory Curiosities to Versatile Reagents in Synthesis
L. Weber, Eur. J. Inorg. Chem. (2017) 3461–3488.
DOI: 10.1002/ejic.201700629
DOI: 10.1002/ejic.201700629
Bis-Gd complexes for solid effect and cross effect dynamic nuclear polarization
M. Kaushik, M. Qi, A. Godt, B. Corzilius, Angew. Chem. Int. Ed. (2017).
DOI: 10.1002/anie.201612388
DOI: 10.1002/anie.201612388
Expanding the Group of Porous Interpenetrated Zr-Organic Frameworks (PIZOFs) with Linkers of Different Lengths
Inorg. Chem. 56 (2017) 748–761.
Gd3+–Gd3+ distances exceeding 3 nm determined by very high frequency continuous wave electron paramagnetic resonance
J. A. Clayton, M. Qi, A. Godt, D. Goldfarb, S. Han, M. S. Sherwin, Phys. Chem. Chem. Phys. 19 (2017) 5127–5136.
CIDME: Short distances measured with long chirp pulses
A. Doll, M. Qi, A. Godt, G. Jeschke, J. Magn. Reson. 273 (2016) 73–82.
Averaging of nuclear modulation artefacts in RIDME experiments
K. Keller, A. Doll, M. Qi, A. Godt, G. Jeschke, M. Yulikov, J. Magn. Reson., 272 (2016) 108–113.
DOI: 10.1016/j.jmr.2016.09.016
DOI: 10.1016/j.jmr.2016.09.016
Nonplanar Polyaromatic Compounds
D. Kuck, Synlett, 27 (2016) 2068–2069.
DOI: 10.1021/jacs.6b05820
DOI: 10.1021/jacs.6b05820
Cover & Spotlight:
Three-Fold Scholl-Type Cycloheptatriene Ring Formation around a Tribenzotriquinacene Core – On the Way to Warped Graphenes
Three-Fold Scholl-Type Cycloheptatriene Ring Formation around a Tribenzotriquinacene Core – On the Way to Warped Graphenes
H.-W. Ip, C.-F. Ng, H.-F. Chow, D. Kuck, J. Am. Chem. Soc., 138 (2016) 13778–13781.
DOI: 10.1021/jacs.6b05820
DOI: 10.1021/jacs.6b05820
Single Functionalization of Fenestrindane and Centrohexaindane at the Molecular Periphery
J. Linke, D. Kuck, Z. Naturforsch. B, 71 (2016) 897–904.
DOI: 10.1515/znb-2016-0067
DOI: 10.1515/znb-2016-0067
Synthesis and Hydrolysis of 4-Chloro-PyMTA and 4-Iodo-PyMTA Esters and Their Oxidative Degradation with Cu(I/II) and Oxygen
M. Qi, M. Hülsmann, A. Godt, Synthesis, 48 (2016) 3773–3784.
DOI: 10.1055/s-0035-1561660
DOI: 10.1055/s-0035-1561660
EPR characterization of Mn(II) complexes for distance determination with pulsed dipolar spectroscopy
K. Keller, M. Zalibera, M. Qi, V. Koch, J. Wegner, H. Hintz, A. Godt, G. Jeschke, A. Savitsky, M. Yulikov, Phys. Chem. Chem. Phys., 18 (2016) 25120–25135.
DOI: 10.1039/c6cp04884f
DOI: 10.1039/c6cp04884f
The Tris(pentafluoroethyl)silanide Anion
N. Schwarze, S. Steinhauer, B. Neumann, H.-G. Stammler, B. Hoge, Angew. Chem. 128 (2016) 16390–16394;; Angew. Chem. Int. Ed. 55 (2016) 16156–16160.
DOI: 10.1002/ange.201609096; 10.1002/anie.201609096 (Int.Ed.)
DOI: 10.1002/ange.201609096; 10.1002/anie.201609096 (Int.Ed.)
Nucleophilic Transfer Reactions of the [Si(C2F5)3]- Moiety
N. Schwarze, S. Steinhauer, B. Neumann, H.-G. Stammler, B. Hoge, Angew. Chem. 128 (2016) 16395–16398; Angew. Chem. Int. Ed. 55 (2016) 16161–16164.
DOI: 10.1002/ange.201609575;10.1002/anie.201609575 (Int.Ed.)
DOI: 10.1002/ange.201609575;10.1002/anie.201609575 (Int.Ed.)
Pentafluoroethylsilicic Acids
N. Schwarze, S. Steinhauer, B. Neumann, H.-G. Stammler, B. Hoge, Angew. Chem. 128 (2016) 15756–15759; Angew. Chem. Int. Ed. 55 (2016) 15528–15530.
DOI: 10.1002/ange.201609097; 10.1002/anie.201609097 (Int.Ed.)
DOI: 10.1002/ange.201609097; 10.1002/anie.201609097 (Int.Ed.)
Synthesis of Functional Bis(pentafluoroethyl)silanes (C2F5)2SiX2,
with X = H, F, Cl, Br, OPh, O2CCF3
with X = H, F, Cl, Br, OPh, O2CCF3
N. Schwarze, B. Kurscheid, S. Steinhauer, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 22 (2016) 17460–17467.
DOI: 10.1002/chem.201603442
DOI: 10.1002/chem.201603442
Hypervalent Pentafluoroethylgermanium Compounds, [(C2F5)nGeX5-n]- and
[(C2F5)3GeF3]2- (X = F, Cl; N = 2–5)
S. Pelzer, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 22 (2016) 16460–16466.
DOI: 10.1002/chem.201602859
DOI: 10.1002/chem.201602859
Novel Difluorotriorganylphosphoranes for the Synthesis of Fluorophosphonium and Bismuthonium salts
S. Solyntjes, B. Neumann, H.-G. Stammler, N. Ignatiev, B. Hoge, Eur. J. Inorg. Chem. (2016) 3999–4010.
DOI: 10.1002/ejic.201600539
DOI: 10.1002/ejic.201600539
Gd(III)-Gd(III) EPR distance measurements - the range of accessible distances and the impact of zero field splitting
A. Dalaloyan, M. Qi, S. Ruthstein, S. Vega, A. Godt, A. Feintuch, D. Goldfarb, Phys. Chem. Chem. Phys., 18 (2016) 18614.
DOI: 10.1039/c6cp90156e
DOI: 10.1039/c6cp90156e
Spacers for Geometrically Well-Defined Water-Soluble Molecular Rulers and Their Application
M. Qi, M. Hülsmann, A. Godt, J. Org. Chem., 81 (2016) 2549–2571.
DOI: 10.1021/acs.joc.6b00125
DOI: 10.1021/acs.joc.6b00125
Gd(III) complexes as paramagnetic tags: Evaluation of the spin delocalization over the nuclei of the ligand
A. Collauto, A. Feintuch, M. Qi, A. Godt, T. Meade, D. Goldfarb, J. Magn. Reson., 263 (2016) 156–163.
DOI: 10.1016/j.jmr.2015.12.025
DOI: 10.1016/j.jmr.2015.12.025
Carbon-based two electron σ-donor ligands beyond classical N-heterocyclic carbenes
R. J. Ghadwal, Dalton Trans., 45 (2016) 16081–16095.
DOI: 10.1039/C6DT02158A
DOI: 10.1039/C6DT02158A
Merging Tribenzotriquinacene and Triptycene
F. Lucchesini, M. Grasse, B. Neumann, H.-G. Stammler, J. Tellenbröker, D. Kuck, Eur. J. Org. Chem. (2016) 2828–2841.
DOI: 10.1002/ejoc.201600176
DOI: 10.1002/ejoc.201600176
A Polycyclic Aromatic Hydrocarbon Bearing an all-cis-Tetrabenzo[5.5.5.5] fenestrane (Fenestrindane) Core Merged with Two Hexa-peri-hexabenzocoronene Units
P. An, H.-F. Chow, D. Kuck, Synlett, 27 (2016) 1255–1261.
DOI: 10.1055/s-0035-1561443
DOI: 10.1055/s-0035-1561443
Surface stabilization determines a classical versus non-classical nucleation pathway during particle formation
A. Dreyer, K. Eckstädt, T. Koop, P. Jutzi, A. Hütten, RSC Advances 6 (2016) 74061–74066.
DOI: 10.1039/C6RA13041K
DOI: 10.1039/C6RA13041K
o-Quinones Derived from Tribenzotriquinacenes: Functionalization of Inner Bay Positions and Use for Single-Wing Extensions
Y.-F. Zhang, W.-F. Tian, X.-P. Cao, D. Kuck, H.-F. Chow, J. Org. Chem., 81 (2016) 2308–2319.
DOI: 10.1021/acs.joc.5b02806
DOI: 10.1021/acs.joc.5b02806
Centrohexaindane: Six Benzene Rings Mutually Fixed in Three Dimensions – Solid-State Structure and Six-fold Nitration
D. Kuck, J. Linke, L. C. Teichmann, D. Barth, J. Tellenbröker, D. Gestmann, B. Neumann, H.-G. Stammler, H. Bögge, Phys. Chem. Chem. Phys., 18 (2016) 11722–11737.
DOI: 10.1039/C5CP07005H
DOI: 10.1039/C5CP07005H
Das Bis(pentafluorethyl)germylen-Trimethylphosphan-Addukt, (C2F5)2Ge·PMe3 - Charakterisierung, Ligandeigenschaften und Reaktivität
S. Pelzer, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Angew. Chem., 128 (2016) 6192–6197; Angew. Chem. Int. Ed., 55 (2016) 6088–6092.
DOI: 10.1002/ange.201601468; 10.1002/anie.201601468 (Int.Ed.)
DOI: 10.1002/ange.201601468; 10.1002/anie.201601468 (Int.Ed.)
Hot Paper:
Synthesis of Bis(pentafluoroethyl)germanes
Synthesis of Bis(pentafluoroethyl)germanes
S. Pelzer, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 22 (2016) 4758–4763.
DOI: 10.1002/chem.201505084
DOI: 10.1002/chem.201505084
Hot Paper:
Synthesis of Tris(pentafluoroethyl)germanes
Synthesis of Tris(pentafluoroethyl)germanes
S. Pelzer, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 22 (2016) 3327–3332.
DOI: 10.1002/chem.201504626
DOI: 10.1002/chem.201504626
Inside Cover:
Trimethylaluminum: Bonding by Charge and Current Topology
Trimethylaluminum: Bonding by Charge and Current Topology
H.-G. Stammler, S. Blomeyer, R. J. F. Berger, N. W. Mitzel, Angew. Chem., 127 (2015), 14021–14026; Angew. Chem. Int. Ed., 54 (2015), 13816–13820.
DOI: 10.1002/ange.201505665; 10.1002/anie.201505665 (Int. Ed.)
DOI: 10.1002/ange.201505665; 10.1002/anie.201505665 (Int. Ed.)
Enantiomerically Pure Tribenzotriquinacenes Through Stereoselective Synthesis
W. Greschner, B. Neumann, H.-G. Stammler, H. Gröger, D. Kuck, Angew. Chem., 127 (2015), 13968–13972; Angew. Chem. Int. Ed., 54 (2015), 13764–13768.
DOI: 10.1002/ange.201506906; 10.1002/anie.201506906 (Int. Ed.)
DOI: 10.1002/ange.201506906; 10.1002/anie.201506906 (Int. Ed.)
Cover & Cover Profile:
Facile Assembly of Chiral Metallosquares Using Enantiopure Tribenzotriquinacene Corner Motifs
Facile Assembly of Chiral Metallosquares Using Enantiopure Tribenzotriquinacene Corner Motifs
W.-R. Xu, G.-J. Xia, H.-F. Chow, X.-P. Cao, D. Kuck, Chem. Eur. J., 21 (2015) 12011–12017.
DOI: 10.1002/chem.201501556
DOI: 10.1002/chem.201501556
Glass formation processes in mixed inorganic/organic aerosol particles
H. P. Dette, T. Koop, J. Phys. Chem. A 119 (2015) 4552–4561.
DOI: 10.1021/jp5106967
DOI: 10.1021/jp5106967
Hot Paper:
Coordination Properties of Perfluoroethyl- and Perfluorophenyl-Substituted Phosphonous acids, RfP(OH)2
Coordination Properties of Perfluoroethyl- and Perfluorophenyl-Substituted Phosphonous acids, RfP(OH)2
N. Allefeld, B. Kurscheid, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 21 (2015) 13666–13675.
DOI: 10.1002/chem.201501984
DOI: 10.1002/chem.201501984
Transition Metal Complexes of Phosphinous Acids Featuring a Quasichelating Unit: Synthesis, Characterization, and Hetero-bimetallic Complexes
N. Allefeld, J. Bader, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Inorg. Chem. 54 (2015) 7945–7952.
DOI: 10.1021/acs.inorgchem.5b01038
DOI: 10.1021/acs.inorgchem.5b01038
Hot Paper + Inside Cover:
Functionalized Pentafluoroethylphosphanes
Functionalized Pentafluoroethylphosphanes
N. Allefeld, B. Neumann, H.-G. Stammler, N. Ignat'ev, B. Hoge, Chem. Eur. J. 21 (2015) 12326–12336.
DOI: 10.1002/chem.201501733
DOI: 10.1002/chem.201501733
Tribenzotriquinacene-based Tris-Cyclophanes: Intra- and Inter-wing C3v-symmetrical Extension of the Bowl-Shaped TBTQ Core
E. U. Mughal, B. Neumann, H.-G. Stammler, Z.-M. Li, J. Wei, D. Kuck, X.-P. Cao, Eur. J. Org. Chem., (2015) 2835–2847.
DOI: 10.1002/ejoc.201500219
DOI: 10.1002/ejoc.201500219
Synthesis and Characterization of 1,2,3,4,5-Pentafluoroferrocene
K. Sünkel, S. Weigand, A. Hoffmann, S. Blomeyer, C. Reuter, Y. V. Vishnevskiy, N. W. Mitzel, J. Am. Chem. Soc., 137(1) (2015) 126–129.
DOI: 10.1021/ja511588p
DOI: 10.1021/ja511588p
The role of 2,3-dihydro-1-H-1,3,2-diazaboroles in luminescent molecules
L. Weber, L. Böhling, Coord. Chem. Rev., 284 (2015) 236–275.
DOI: 10.1016/j.ccr.2014.09.022
DOI: 10.1016/j.ccr.2014.09.022
Hemi- and holo-directed lead(II) complexes in a soft ligand environment
M. Imran, A. Mix, B. Neumann, H.-G. Stammler, U. Monkowius, P. Gründlinger, N. W. Mitzel, Dalton Trans., 44 (2015) 924–937.
DOI: 10.1039/C4DT01406E
DOI: 10.1039/C4DT01406E
Gd(III)-Gd(III) distance measurements with chirp pump pulses
A. Doll, M. Qi, N. Wili, S. Pribitzer, A. Godt, G. Jeschke, J. Magn. Reson., 253 (2015) 153–162.
DOI: 10.1016/j.jmr.2015.08.010
DOI: 10.1016/j.jmr.2015.08.010
Gd(III)-Gd(III) EPR distance measurements - the range of accessible distances and the impact of zero field splitting
A. Dalaloyan, M. Qi, S. Ruthstein, S. Vega, A. Godt, A. Feintuch, D. Goldfarb, Phys. Chem. Chem. Phys., 17 (2015) 18464–18476.
DOI: 10.1039/c5cp02602d
DOI: 10.1039/c5cp02602d
Sensitivity enhancement by population transfer in Gd(III) spin labels
A. Doll, M. Qi, S. Pribitzer, N. Wili, M. Yulikov, A. Godt, G. Jeschke, Phys. Chem. Chem. Phys., 17 (2015) 7334–7344.
DOI: 10.1039/c4cp05893c
DOI: 10.1039/c4cp05893c
Solid-State Structure of a Li⁄F-Carbenoid: Pentafluoroethyllithium
B. Waerder, S. Steinhauer, B. Neumann, H.-G. Stammler, A. Mix, Y. V. Vishnevskiy, B. Hoge, N. W. Mitzel, Angew. Chem., 126 (2014), 11824–11828;
Angew. Chem. Int. Ed., 53 (2014) 11640–11644.
DOI: 10.1002/ange.201406564; 10.1002/anie.201406564 (Int.Ed.)
DOI: 10.1002/ange.201406564; 10.1002/anie.201406564 (Int.Ed.)
Gd(III)-PyMTA Label Is Suitable for In-Cell EPR
M. Qi, A. Groß, G. Jeschke, A. Godt, M. Drescher, J. Am. Chem. Soc., 136 (2014) 15366–15378.
DOI: 10.1021/ja508274d
DOI: 10.1021/ja508274d
RIDME Spectroscopy with Gd(III) Centers
S. Razzaghi, M. Qi, A. I. Nalepa, A. Godt, G. Jeschke, A. Savitsky, M. Yulikov, J. Phys. Chem. Lett., 5 (2014) 3970–3975.
DOI: 10.1021/jz502129t
DOI: 10.1021/jz502129t
Quantitative Efficacy Classification of Ice Recrystallization Inhibition Agents
C. Budke, A. Dreyer, J. Jaeger, K. Gimpel, T. Berkemeier, A. S. Bonin, L. Nagel, C. Plattner, A. L. DeVries, N. Sewald, T. Koop, Cryst. Growth Des., 14 (2014) 4285–4294.
DOI: 10.1021/cg5003308
DOI: 10.1021/cg5003308
Glass-Forming Properties of 3-Methylbutane-1,2,3-tricarboxylic Acid and Its Mixtures with Water and Pinonic Acid
H. P. Dette, M. Qi, D. C. Schröder, A. Godt, T. Koop, J. Phys. Chem. A, 118 (2014) 7024–7033.
DOI: 10.1021/jp505910w
DOI: 10.1021/jp505910w
Alkynyl Compounds of the Rare-earth Metals
A. Nieland, J.-H. Lamm, A. Mix, B. Neumann, H.-G. Stammler, N. W. Mitzel, Z. Anorg. Allg. Chem., 640 (2014) 2484–2491.
DOI: 10.1002/zaac.201400158
DOI: 10.1002/zaac.201400158
Poly-Boron, -Silicon, and -Gallium Lewis Acids by Hydrometallation of 1,5- and 1,8-Dialkynylanthracenes
J.-H. Lamm, J. Horstmann, J. H. Nissen, J.-H. Weddeling, B. Neumann, H.-G. Stammler, N. W. Mitzel, Eur. J. Inorg. Chem., 26 (2014) 4294–4301.
DOI: 10.1002/ejic.201402376
DOI: 10.1002/ejic.201402376
Synthesis, structural and photo-physical studies of bismuth(III) complexes with Janus scorpionate and co-ligands
M. Imran, A. Mix, B. Neumann, H.-G. Stammler, U. Monkowius, P. Bleckenwegner, N. W. Mitzel, Dalton Trans., 43 (2014) 10956–10968.
DOI: 10.1039/C4DT00668B
DOI: 10.1039/C4DT00668B
Cover:
Synthesis of Unsymmetrically Substituted Phosphane Oxides (R1R2P(O)H) and Phosphinous Acids (R1R2POH)
Synthesis of Unsymmetrically Substituted Phosphane Oxides (R1R2P(O)H) and Phosphinous Acids (R1R2POH)
N. Allefeld, M. Grasse, N. Ignat'ev, B Hoge, Chem. Eur. J., 20 (2014) 8615–8620.
DOI: 10.1002/chem.201402425
DOI: 10.1002/chem.201402425
Back Cover:
Synthesis and Reactivity of New Functionalized Perfluoroalkylfluorophosphates
Synthesis and Reactivity of New Functionalized Perfluoroalkylfluorophosphates
N. Allefeld, B. Neumann, H.-G. Stammler, G.-V. Röschenthaler, N. Ignat'ev, B Hoge, Chem. Eur. J., 20 (2014) 7736–7745.
DOI: 10.1002/chem.201402421
DOI: 10.1002/chem.201402421
Inside Back Cover:
Pentacoordinate silicon(IV): cationic, anionic and neutral complexes derived from the reaction of NHC→SiCl4 with highly Lewis acidic (C2F5)2SiH2
Pentacoordinate silicon(IV): cationic, anionic and neutral complexes derived from the reaction of NHC→SiCl4 with highly Lewis acidic (C2F5)2SiH2
T. Böttcher, S. Steinhauer, B. Neumann, H.-G. Stammler, G.-V. Röschenthaler, B. Hoge, Chem. Commun., 50 (2014) 6204–6206.
DOI: 10.1039/C4CC02583K
DOI: 10.1039/C4CC02583K
Synthesis of Chlorosilicates
S. Steinhauer, T. Böttcher, N. Schwarze, B. Neumann, H.-G. Stammler, B. Hoge, Angew. Chem., 126 (2014), 13485–13488; Angew. Chem. Int. Ed.,
53 (2014), 13269–13272.
DOI: 10.1002/ange.201406311; DOI: 10.1002/anie.201406311 (Int. Ed.)
DOI: 10.1002/ange.201406311; DOI: 10.1002/anie.201406311 (Int. Ed.)
Synthesis of Functional Phosphates [P(C2F5)3F2X]- from the Phosphorane Adduct
[P(C2F5)3F2(dmap)]
J. Bader, N. Ignat'ev, B. Hoge, Inorg. Chem., 53 (2014) 7547–7553.
DOI: 10.1021/ic500857b
DOI: 10.1021/ic500857b