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

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

Back Cover:
Dodecabromo- and Dodecaiodocentrohexaindane: T_d-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

Cover:
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

Feature Article:
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

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

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

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

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

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

Reviews Showcase:
Pentafluoroethylated Compounds of Silicon, Germanium and Tin

M. Wiesemann, B. Hoge, Chem. Eur. J. 24 (2018) im Druck.
DOI: 10.1002/chem.201801292

Hot Paper + Cover Feature:
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

Hot Paper:
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

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

VIP:
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

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

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

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

Hot Paper + Cover Feature:
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

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.)

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

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

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

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

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

Hot Paper + Cover Feature:
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

VIP + Front Cover + Cover Profile:
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

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

Synthesis of Mono-, Bis- and Tris(pentafluoroethyl)tin Derivatives, (C₂F₅)_4–nSnX_n (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

Feature:
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

Hot Paper:
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

Hot Paper + Back Cover:
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

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

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

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

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

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

Nonplanar Polyaromatic Compounds

D. Kuck, Synlett, 27 (2016) 2068–2069.
DOI: 10.1021/jacs.6b05820

Cover & Spotlight:
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

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

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

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

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.)

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.)

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.)

Synthesis of Functional Bis(pentafluoroethyl)silanes (C₂F₅)₂SiX₂,
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

Hypervalent Pentafluoroethylgermanium Compounds, [(C₂F₅)_nGeX_5-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

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

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

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

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

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

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

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

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

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

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

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.)

Hot Paper:
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

Hot Paper:
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

Inside Cover:
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.)

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.)

Cover & Cover Profile:
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

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

Hot Paper:
Coordination Properties of Perfluoroethyl- and Perfluorophenyl-Substituted Phosphonous acids, R^fP(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

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

Hot Paper + Inside Cover:
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

Tribenzotriquinacene-based Tris-Cyclophanes: Intra- and Inter-wing C_3v-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

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

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

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

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

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

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

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.)

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

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

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

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

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

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

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

Cover:
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

Back Cover:
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

Inside Back Cover:
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

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.)

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