Search results for "BIP"
showing 10 items of 1908 documents
Packing colorings of subcubic outerplanar graphs
2018
Given a graph $G$ and a nondecreasing sequence $S=(s_1,\ldots,s_k)$ of positive integers, the mapping $c:V(G)\longrightarrow \{1,\ldots,k\}$ is called an $S$-packing coloring of $G$ if for any two distinct vertices $x$ and $y$ in $c^{-1}(i)$, the distance between $x$ and $y$ is greater than $s_i$. The smallest integer $k$ such that there exists a $(1,2,\ldots,k)$-packing coloring of a graph $G$ is called the packing chromatic number of $G$, denoted $\chi_{\rho}(G)$. The question of boundedness of the packing chromatic number in the class of subcubic (planar) graphs was investigated in several earlier papers; recently it was established that the invariant is unbounded in the class of all sub…
CCDC 1014200: Experimental Crystal Structure Determination
2014
Related Article: Hai Yi, Markus Albrecht, Arto Valkonen, Kari Rissanen|2015|New J.Chem.|39|746|doi:10.1039/C4NJ01654H
CCDC 1525503: Experimental Crystal Structure Determination
2017
Related Article: Ngong Kodiah Beyeh, Hyun Hwa Jo, Igor Kolesnichenko, Fangfang Pan, Elina Kalenius, Eric V. Anslyn, Robin H. A. Ras, Kari Rissanen|2017|J.Org.Chem.|82|5198|doi:10.1021/acs.joc.7b00449
Crystal and solution structures of di-n-butyltin(IV) complexes of 5-[(E)-2-(4-methoxyphenyl)-1-diazenyl]quinolin-8-ol and benzoic acid derivatives: E…
2009
Abstract Reactions of nBu2SnCl(L1) (1), where L1 = acid residue of 5-[(E)-2-(4-methoxyphenyl)-1-diazenyl]quinolin-8-ol, with various substituted benzoic acids in refluxing toluene, in the presence of triethylamine, yielded dimeric mixed ligand di-n-butyltin(IV) complexes of composition [nBu2Sn(L1)(L2–6)]2 where L2 = benzene carboxylate (2), L3 = 2-[(E)-2-(2-hydroxy-5-methylphenyl)-1-diazenyl]benzoate (3), L4 = 5-[(E)-2-(4-methylphenyl)-1-diazenyl]-2-hydroxybenzoate (4), L5 = 2-{(E)-4-hydroxy-3-[(E)-4-chlorophenyliminomethyl]-phenyldiazenyl}benzoate (5) and L6 = 2-[(E)-(3-formyl-4-hydroxyphenyl)-diazenyl]benzoate (6). All complexes (1–6) have been characterized by elemental analyses, IR, 1H,…
CCDC 1008816: Experimental Crystal Structure Determination
2015
Related Article: Bernd Elsler, Anton Wiebe, Dieter Schollmeyer, Katrin M. Dyballa, Robert Franke, Siegfried R. Waldvogel|2015|Chem.-Eur.J.|21|12321|doi:10.1002/chem.201501604
CCDC 1864309: Experimental Crystal Structure Determination
2018
Related Article: B. Dziuk, A. Jezuita|2018|IUCrData|3|x181219|doi:10.1107/S2414314618012191
CCDC 780779: Experimental Crystal Structure Determination
2013
Related Article: F.Emmerling, I.Orgzall, B.Dietzel, B.Schulz, J.Larrucea|2012|J.Mol.Struct.|1030|209|doi:10.1016/j.molstruc.2012.04.040
CCDC 780778: Experimental Crystal Structure Determination
2013
Related Article: F.Emmerling, I.Orgzall, B.Dietzel, B.Schulz, J.Larrucea|2012|J.Mol.Struct.|1030|209|doi:10.1016/j.molstruc.2012.04.040
Preparation and structural characterization of organotin(IV) complexes with ligands containing a hetero {N} atom and a hydroxy group or hydroxy and c…
2005
AbstractTwenty-two n-butyltin(IV) and t-butyltin(IV) complexes of ligands containing an –OH (–C@O) group or –OH and –COOHgroups and an aromatic {N} donor atom were prepared by metathetical reactions. On the basis of the FT-IR and Mo¨ssbauer spec-troscopic data, molecular structures were assigned to these compounds. The binding sites of the ligands were identified by means ofFT-IR spectroscopic measurements, and it was found that in most cases the organotin(IV) moiety reacts with the phenolic form ofthese ligands. In the complexes with –OH and –COOH functions, the –COOH group is coordinated to the organotin(IV) centres in amonodentate manner. The 119 Sn Mo¨ssbauer and the FT-IR studies suppor…
CCDC 784160: Experimental Crystal Structure Determination
2011
Related Article: R.Francke, G.Schnakenburg, S.R.Waldvogel|2010|Org.Lett.|12|4288|doi:10.1021/ol101698a