3 research outputs found
Synthesis and Structure of the Bis- and Tris-Polyhedral Hybrid Carboranoclathrochelates with Functionalizing Biorelevant Substituents—The Derivatives of Propargylamine Iron(II) Clathrochelates with Terminal Triple C≡C Bond(s)
- Author
- Publication venue
- 'MDPI AG'
- Publication date
- 01/06/2021
- Field of study
A synthetic strategy for obtaining structurally flexible hybrid iron(II) carboranoclatrochelates functionalized with biorelevant groups, based on a combination of a 1,3-dipolar cycloaddition reaction with nucleophilic substitution of an appropriate chloroclathrochelate precursor, was developed. In its first stage, a stepwise substitution of the dichloroclathrochelate precursor with amine N-nucleophiles of different natures in various solvents was performed. One of its two chlorine atoms with morpholine or diethylamine in dichloromethane gave reactive monohalogenoclathrochelate complexes functionalized with abiorelevant substituents. Further nucleophilic substitution of their remaining chlorine atoms with propargylamine in DMF led to morpholine- and diethylamine-functionalized monopropargylamine cage complexes, the molecules of which contain the single terminal C≡C bond. Their “click” 1,3-cycloaddition reactions in toluene with ortho-carborane-(1)-methylazide catalyzed by copper(II) acetate gave spacer-containing di- and tritopic iron(II) carboranoclatrochelates formed by a covalent linking between their different polyhedral(cage) fragments. The obtained complexes were characterized using elemental analysis, MALDI-TOF mass, UV-Vis, 1H, 1H{11B}, 11B, 11B{1H}, 19F{1H} and 13C{1H}-NMR spectra, and by a single crystal synchrotron X-ray diffraction experiment for the diethylamine-functionalized iron(II) carboranoclathrochelate. Its encapsulated iron(II) ion is situated almost in the center of the FeN6-coordination polyhedron possessing a geometry intermediate between a trigonal prism and a trigonal antiprism with a distortion angle φ of approximately 28°. Conformation of this hybrid molecule is strongly affected by its intramolecular dihydrogen bonding: a flexibility of the carborane-terminated ribbed substituent allowed the formation of numerous C–H…H–B intramolecular interactions. The H(C) atom of this carborane core also forms the intermolecular C–H…F–B interaction with an adjacent carboranoclathrochelate molecule. The N–H…N intermolecular interaction between the diethylamine group of one hybrid molecule and the heterocyclic five-membered 1H-[1,2,3]-triazolyl fragment of the second molecule of this type caused formation of H-bonded carboranoclathrochelate dimers in the X-rayed crystal
An efficient synthesis of carboranyl tetrazoles via alkylation of 5-R-1H-tetrazoles with allylcarboranes
- Author
- Alexander S. Peregudov
- Alterman
- Amantini
- Anton V. Makarenkov
- Aridoss
- Athanassopoulos
- Aureggi
- Bekhit
- Bhaskar
- Borah
- Brase
- Clovis
- Coca
- Demarinis
- Demko
- Demko
- Dunica
- Efimova
- El Kaim
- Elena G. Kononova
- Enders
- Farha
- Fettes
- Frija
- Gaponik
- Gaponik
- Ghirotti
- Grimes
- Gupta
- Hajra
- Han
- Hawthorne
- Hayao
- Herr
- Hert
- Himo
- Jankowski
- Kalinin
- Kalinin
- Kamijo
- Keith
- Koldobskii
- Koldovskii
- Konstantin A. Lyssenko
- Koren
- Koren
- Koren
- Koren
- Kukushkin
- Lee
- Maleki
- Matta
- Maxwell
- McKie
- Mohite
- Murphy
- Murphy
- Naumenko
- Nelson
- Olid
- Ol’shevskaya
- Ol’shevskaya
- Ol’shevskaya
- Palazzi
- Pande
- Piecek
- Potts
- Quintin
- Roh
- Roh
- Sandmann
- Sarvary
- Schnermann
- Schwab
- Sesha
- Sheldrick
- Shie
- Song
- Song
- Sun
- Teixidor
- Terashima
- Toubro
- Touti
- Upadhayaya
- Valentina A. Ol’shevskaya
- Valery N. Kalinin
- Valliant
- Wee
- Wee
- Weinberg
- Wittenberger
- Wittenberger
- Xamena
- Yu
- Zakharkin
- Zakharkin
- Zakharkin
- Zhan
- Zubarev
- Publication venue
- 'Elsevier BV'
- Publication date
- Field of study
CMS TriDAS project: Technical Design Report, Volume 1: The Trigger Systems
- Author
- Aarnio Pertti A
- Abadjiev K
- Abbaneo D
- Abbrescia M
- Abdullin S
- Abramov A
- Abramov V
- Acharya B S
- Acosta D
- Adam W
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- Adzic P
- Afanasiev S V
- Aftab Z
- Ageron M
- Aguilar-BenĂtez M
- Ahmad J R
- Ahmad M A
- Ahn S
- Akchurin N
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- Almeida C
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- Altieri S
- Alverson G
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- Amsler Claude
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- Maazouzi C
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- MacFarlane D
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- Nagaslaev V
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- Navarria Francesco Luigi
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- Ostapchuk A Ya
- Otwinowski S
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- Pal I
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- Palla F
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- Pandoulas D
- Panov V
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- Panyam N
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- Papadimitriou V
- Papageorgiou K
- Pape L
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- Passardi Giorgio
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- Patalakha D I
- Patil M R
- Patino-Revuelta A
- Patrick J
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- Paus C
- Pauss Felicitas
- Pavlon S
- Pavlov I
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- Peisert Anna
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- Penchev L
- Perelygin V P
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- Pernicka Manfred
- Peroni C
- Perriès S
- Perrotta A
- Petagna P
- Petertill M
- Petev P
- Petrouchanko S
- Petrov V
- Petrunin A
- Petukhov Yu P
- Pfeiffer A
- Pieri M
- Pierschel G
- Pietarinen E
- Pietrusinski M
- Pikalov V A
- Pimiä Martti
- Pintus R
- Piotrzkowski K
- Piotto E
- Pirollet B
- Pirollo S
- Piroué P A
- Pishchalnikov Yu M
- Placci Alfredo
- Placidi P
- Platner E D
- Podrasky V
- Poilleux P
- Poliarouch A
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- Pordes R
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- Potapov V
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- Principe R
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- Prokofiev O E
- Proskouriakov A
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- Prosper H B
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- Pruys H S
- Puccini M
- Puerta-Pelayo J
- Pugliese G
- Puljak I
- Punzi G
- Pálinkás J
- Pásztor G
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- Qiu J F
- Quadt A
- Rabbetts P D
- Radicci V
- Raffaelli F
- Rahal G
- Raics P
- Raidal Martti
- Raja R
- Rakhmatov N
- Ramond P
- Ramos S
- Rander J
- Ranieri A
- Rapidis P A
- Rasmislovich V
- Ratti S P
- Raupach F
- Raven G
- Raykov P
- Raymond D M
- Razis P A
- Razmyslovich B V
- Rebecchi P
- Reeder D
- Regenfus C
- Reichanadter M
- Reidy J
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- Reymond J M
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- Rodrigues-Simoes-Moreira P
- Rohe T
- Rohlf J
- Rohringer Herbert
- Roinishvili N N
- Roinishvili V N
- Rolandi Luigi
- Romano F
- Romanteau T
- Romero A
- Romero L
- Ronchese P
- Rondeaux F
- Ronzhin A
- Rosca A
- Rosenson L
- Rosowsky A
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- Rusack R W
- Rusakov S V
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- Russ J
- Russo V
- Rustamov I
- Ruuskanen P V
- Rykaczewski H
- Rykalin V I
- Rácz A
- Röderer F
- Röser U
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- Sadovskii A
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- Sakhelashvili T M
- Sakulin H
- Sakumoto W
- Salicio J
- Samar A
- Samarine S
- Samoshkin A
- Samyn D
- Sanders D
- Sanguinetti G
- Sannikov A V
- Santiard Jean-Claude
- Santinelli R
- Santocchia A
- Santos M
- Sanzeni C
- Sarycheva L I
- Savage P J
- Savina M V
- Schael S
- Schleifer W
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- Schmidt I
- Schmidt R
- Schmitz D
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- Schneegans M
- Schnetzer S
- Schnyder R
- Schröder M
- Schulte R
- Schultz von Dratzig A
- Schwick C
- Schöning A
- SciabĂ A
- Sciortino S
- Scorzoni A
- Scurlock B
- Seberini M
- Sedov A
- Seez Christopher J
- Segneri G
- Sehgal V
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- Semeniouk I N
- Sempere-Roldan P
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- Sergeev S
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- Shevchenko S
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- Shivpuri R K
- Shmatkov V
- Shmatov S V
- Shri C S
- Shukrullo I
- Siedling R
- Siegrist P
- Siklér F
- Sill A F
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- Simma A
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- Simonis H J
- Simonova Z
- Sinanis N
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- Singovsky A V
- Siotis I
- Siroli G P
- Sirunyan A M
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- Staiano A
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- Staveris-Polykalas A
- Stavitski I
- Stefanescu J
- Steiner S
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- Teixeira I
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- Tseng J
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- Tudoric-Ghemo J
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- TĂłth N
- Udo Fred
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- Uzhinskii V V
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- Vainio O
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- Veltchev I
- Vemuri N
- Ventura L
- Ventura Sandro
- Venturi A
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- Verdini P G
- Verlato M
- Verma P
- Verma V K
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- Vesztergombi G
- Vidal R
- Viertel Gert M
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- Vila I
- Vintache D
- Virdee Tejinder S
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- Wallraff W
- Walsham P
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- Weiler Thomas J
- Weingarten Wolfgang
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- Wertelaers Piet
- Weseler S
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- Willers Ian Malcolm
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- Wittmer B
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- Wrochna G
- Wu Wei Min
- Wu J
- Wu S
- Wulz Claudia Elisabeth
- Wynhoff S
- Xia L
- Xie X
- Xie Z
- Xu Rong Sheng
- Xue Z L
- Yagil A
- Yang M
- Yarba V A
- Yasuda T
- Ye Shu Wei
- Ye Yan Lin
- Yelton J
- Yepes P
- Yildiz H D
- Yuan H B
- Yukaev A I
- Yuldashev B S
- Zach F
- Zachariadou K
- Zaichenko A A
- Zalessky V B
- Zalewski Piotr
- Zalyubovskij I I
- Zamiatin N I
- Zander A
- Zanet A
- Zarubin A V
- Zarubin P I
- Zavodthikov S
- Zeb J
- Zelepoukine S
- Zer-Zion D
- Zeyrek M T
- Zghiche A
- Zhang Bing Yun
- Zhang J W
- Zhang S Q
- Zhang Z P
- Zhao Wei Ren
- Zhao Z
- Zheng Jian Ping
- Zhu G Y
- Zhu R Y
- Zhu Y S
- Zhukov V
- Zilizi G
- Zito G
- Zotto P L
- Zsenei M
- Zubarev E V
- Zullo A
- Zumerle G
- Zupan M
- Zuyeuski R
- Zych P
- Zálán P
- Äystö J
- Ă“dor G
- Ă–nel Y M
- Publication venue
- Publication date
- 22/01/2004
- Field of study