Results 231 to 240 of about 18,040 (292)

Evaluating the halogen bonding strength of a iodoloisoxazolium(III) salt. [PDF]

Beilstein J Org Chem
Reinhard DL, Schmidt A, Sons M, Wolf J, Engelage E, Huber SM.   +5 more
europepmc   +1 more source

The nature of halogen bonding: insights from interacting quantum atoms and source function studies. [PDF]

IUCrJ
Pisati A, Forni A, Pieraccini S, Sironi M.   +3 more
europepmc   +1 more source

A Dual Catalytic Approach for the Halogen-Bonding-Mediated Reductive Cleavage of α-Bromodifluoroesters and Amides. [PDF]

J Org Chem
Tasnim T, Shafiei N, Laminack KJ, Robertson BS, Nevels NE, Fennell CJ, Pitre SP.   +6 more
europepmc   +1 more source

Twist and Shine: The Impact of Halogen Substitution on Thiele Hydrocarbon's Optical Properties

Angewandte Chemie, EarlyView.
Halogenation in Thiele hydrocarbons strongly influences structure and excited‐state dynamics. Depending on substitution, “boat” folded forms show large Stokes shifts and strong solvatochromism, while planar “butterfly” derivatives exhibit near‐unity photoluminescence yields.
Angela Punzi, Tobias Ullrich, Michele Orza, Davide Mesto, Anna Moliterni, Vincent Olieric, Sylvain Engilberge, Cinzia Giannini, Fabrizia Negri, Dirk M. Guldi, Davide Blasi, Gianluca M. Farinola   +11 more
wiley   +1 more source

Asymmetric synthesis of β-amino cyanoesters with contiguous tetrasubstituted carbon centers by halogen-bonding catalysis with chiral halonium salt. [PDF]

Beilstein J Org Chem
Yoshida Y, Aono M, Mino T, Sakamoto M.
europepmc   +1 more source

50 Years of Giese Reaction – a Personal View

Angewandte Chemie, EarlyView.
The Giese‐Reaction celebrates its 50. Birthday, it is a cyclic radical chain reaction centered around C,C‐bond formation in a three component synthesis. This minireview speaks about the birth of the name‐reaction, explains how the complete understanding of its reaction mechanism stimulates new methods in organic synthesis, and why it can proceed in ...
Martin Spichty, Hendrik Zipse, Salem Majouri, Katharina M. Fromm, Bernd Giese   +4 more
wiley   +1 more source

Redox-Responsive Halogen Bonding as a Highly Selective Interaction for Electrochemical Separations. [PDF]

JACS Au
Kim N, Jeyaraj VS, Elbert J, Seo SJ, Mironenko AV, Su X.   +5 more
europepmc   +1 more source

Halogen bonding-based anion coordination in calixarene/inorganic halide/diiodoperfluorocarbon assemblies

, 2009
S. Biella, Giuseppe Gattuso, Anna Notti, Pierangelo Metrangolo, Sebastiano Pappalardo, Melchiorre F. Parisi, Tullio Pilati, Giuseppe Resnati, Giancarlo Terraneo   +8 more
openalex   +2 more sources

A Precisely Bromo‐Functionalized [9]Cycloparaphenylene as a Platform for Late‐Stage Multisite π‐Extension Toward Chiral Nanohoops

Angewandte Chemie, EarlyView.
Precisely synthesized hexabrominated [9]cycloparaphenylene (CPP), accessed by a gold‐mediated method, enables efficient multisite post‐functionalization through cross‐coupling reactions. Late‐stage π‐extension on the CPP framework successfully affords armchair‐type chiral nanohoops exhibiting strong circularly polarized luminescence (|glum| = 0.100 ...
Naoya Kinoshita, Nanami Kotani, Masaya Sugiura, Kotaro Matsumura, Daisuke Sakamaki, Daiki Tauchi, Masashi Hasegawa, Hidetoshi Kawai, Yoshitaka Tsuchido   +8 more
wiley   +1 more source

Predictive, Data‐Driven Design of Red‐Light Photoredox Catalysts for C─Heteroatom Bond Formation

Angewandte Chemie, EarlyView.
From redox numbers to red light: Donor oxidation and core reduction potentials predict E0‐0 in cyanoarene dyes, guiding selection of an efficient red‐light catalyst, 4MeODPATPN (PC13). Under 620 nm light, PC13 facilitates Ni‐catalyzed C─heteroatom cross‐couplings (C─N, C─O, C─S) with high functional‐group tolerance and reduced hydrodehalogenation ...
Amir Gizatullin, Tingting Yuan, Sascha Grotjahn, Luigi Cavallo, Burkhard König, Chen Zhu, Magnus Rueping   +6 more
wiley   +1 more source